supplementhackr
I & I Products Inc.

Done Rite hand sanitizer

LNHPD
24524370
Brand context
I & I Products Inc.
CA
Catalog
1
products
With avoid flag
0
products
FDA recalls
92
history
CAERS
0
reports
Recall historyObjective label signals
Flagged excipients
0
none
FDA recalls
20
20 Class I / II
CAERS reports
0
FDA consumer events
Certifications
0
none recorded
20 FDA recalls on file. · Every flag below links to the authority's published citation.

Supplement Facts

1 active ingredients
IngredientAmount% DV
2-Propanol
other
70.0 % (v/v)—
Recall history

20 FDA recalls

  1. Class II2021-10-01brand-level

    Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tablets, white bottle, NSE Products Inc., Provo, UT 84601 1-888-PHARMANEX

    Reason: Pharmanex Jungamals was found to have a missing fish allergen statement on the label due to fish gelatin as a sub-component of the Vitamin E ingredient.

    FDA record →
  2. Class II2020-01-21brand-level

    All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.

    Reason: Firm ordered by consent decree to recall all products because the products were prepared, packed, or held in violation of current good manufacturing practice regulation (cGMP).

    FDA record →
  3. Class II2015-10-13brand-level

    Oyster Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  4. Class II2015-10-13brand-level

    Esclewe Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  5. Class II2015-10-13brand-level

    Chromium Picolinate Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  6. Class II2015-10-13brand-level

    Sugar Burner Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  7. Class II2015-10-13brand-level

    Blanc Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  8. Class II2015-10-13brand-level

    Gluco + Chond + MSM, Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  9. Class II2015-10-13brand-level

    Extra Mega Prostamax Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  10. Class II2015-10-13brand-level

    Glow Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  11. Class II2015-10-13brand-level

    Bioxtron Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  12. Class II2015-10-13brand-level

    Magic Memory Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  13. Class II2015-10-13brand-level

    Yohimbe Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  14. Class II2015-10-13brand-level

    Tevass 2 Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  15. Class II2015-10-13brand-level

    Prostamax Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  16. Class II2015-10-13brand-level

    Super Inmuno Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  17. Class II2015-10-13brand-level

    Tevass Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  18. Class II2015-10-13brand-level

    Asey Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  19. Class II2015-10-13brand-level

    Shilaji Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →
  20. Class II2015-10-13brand-level

    ADAG Dietary Supplement (unknown container size)

    Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

    FDA record →