Panthera

Primal Pump

Serving
2 Tablet(s)
Per container
60
Form
tablet
DSLD
Formula hash
b5547b214076
Brand context
Catalog
5
products
With avoid flag
3
products
FDA recalls
0
history
CAERS
1
reports
Avoid-flaggedObjective label signals
Flagged excipients
1
1 avoid · 0 caution
FDA recalls
0
no recall history
CAERS reports
1
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

16 active ingredients
IngredientAmount% DV
L-Arginine AKG Primal NOA Driver
Blend (Vitamin)other
3100 mg
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
3 mg150%
Folate
vitaminUNII · 935E97BOY8
UL · set2 effects
600 mcg150%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
60 mg100%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
300 mcg50%
Primal Pump Matrix
Blend (Combination)other
690 mg
Citrulin Maleate
Citrulline malateherb
0 Not Present
Horny Goat Weed
Epimediumherb
0 Not Present
Niacinamide
NiacinvitaminUNII · 25X51I8RD4
UL · set3 effects
0 Not Present
L-Taurine
Taurineherb
0 Not Present
L-Tyrosine
Tyrosineamino_acidUNII · 42HK56048U
0 Not Present
Beta-Alanine
amino_acidUNII · 11P2JDE17B
0 Not Present
Primal Pump Extend Release Matrix
Blend (Combination)other
1050 mg
Di Calcium Phosphate
Calciummineral
UL · set6 effects
0 Not Present
Di Potassium Phosphate
Potassiummineral
3 effects
0 Not Present
Methocel
TBDother
0 Not Present
What this product supports · authorized claims

15 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.

Flagged excipients

1 flagged · authority citations

  • ● AVOIDTitanium Dioxide
    color

    Banned in EU food products effective 2022-08 (Commission Regulation (EU) 2022/63) following EFSA Panel opinion that a safe daily intake could not be established due to genotoxicity concerns. Still GRAS in the US under 21 CFR 73.575 but EU position is stricter.

FDA CAERS · adverse event context
1
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 →

Other ingredients

Magnesium Stearate · Hydroxypropyl Methyl Cellulose · Red 40 · Yellow 6