Garden Of Life

Perfect Food Alkalizer & Detoxifier

Serving
9 Gram(s)
Per container
30
Form
powder
DSLD
Recall historyObjective label signals
Flagged excipients
0
none
FDA recalls
2
2 Class I / II
CAERS reports
8
FDA consumer events
Certifications
0
none recorded
2 FDA recalls on file. · Every flag below links to the authority's published citation.

Supplement Facts

20 active ingredients
IngredientAmount% DV
Calories
UNII · 1
25 {Calories}
Total Carbohydrates
CarbohydrateUNII · 0
5 Gram(s)2%
Sodium
UNII · 9NEZ333N27
60 mg2%
Protein
Protein (unspecified)
1 Gram(s)4%
Vitamin A
UNII · 81G40H8B0T
500 IU10%
Vitamin C
UNII · PQ6CK8PD0R
30 mg50%
Vitamin E
UNII · H4N855PNZ1
15 IU50%
Thiamine
ThiaminUNII · X66NSO3N35
0.135 mg10%
Vitamin B6
UNII · KV2JZ1BI6Z
1.1× ULexceeds NIH ODS adult upper limitsource →
0.108 Gram(s)8%
Calcium
UNII · SY7Q814VUP
150 mg16%
Iron
UNII · E1UOL152H7
7 mg40%
Magnesium
UNII · I38ZP9992A
30 mg10%
Chromium
UNII · 0R0008Q3JB
120 mcg100%
Potassium
UNII · RWP5GA015D
230 mg6%
RAW Organic U.S.A. Farmed Green Juice Blend
Blend (Herb/Botanical)
3.2 Gram(s)
RAW Organic Alkalizer Blend
Blend (Combination)
3 Gram(s)
Organic Detoxifier Blend
Blend (Herb/Botanical)
1.1 Gram(s)
RAW Organic Fruit & Veggie Juice Antioxidant Blend
Blend (Herb/Botanical)
1.1 Gram(s)
RAW Organic Sprout Blend
Blend (Herb/Botanical)
1 Gram(s)
Calories
UNII · 1
100 mg
What this product supports · authorized claims

22 authority-backed effects

Rolled up from EFSA / FDA / NIH ODS authorized function claims on this product's active ingredients. Each row shows which ingredients contribute.

Recall history

2 FDA recalls

  1. Class II2023-10-19brand-level

    Garden of Life, RM-10, Organically Grown Mushrooms, 60 Vegetarian Caplets, Whole Food Dietary Supplement

    Reason: Undeclared Soy.

    FDA record →
  2. Class I2017-09-07brand-level

    Garden of Life, Baby Organic Liquid probiotic formula, 56 ml (1.9 fl oz)

    Reason: The product may pose a choking hazard to newborns due to the thickness of the liquid.

    FDA record →
FDA CAERS · adverse event context
8
consumer-submitted adverse event reports filed with the FDA CFSAN Adverse Event Reporting System mentioning this product or its brand.

CAERS reports are unverified consumer submissions — not adjudicated causality. Large well-known brands accumulate proportionally more reports simply due to broader use. About CAERS →

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.