Otc - Purpose
| Active Ingredient | Purpose |
|---|---|
| Histamine Dihydrochloride 0.028% | Topical Analgesic |
| Menthol 4.574% | Topical Analgesic |
The following Structured Product Label (SPL) was submitted to the FDA by Family First Pharmaceuticals, Inc. for the product Activon Ultra Strength Arthritis (NDC 51068-501). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor if, otc - pregnancy or breast feeding, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
| Active Ingredient | Purpose |
|---|---|
| Histamine Dihydrochloride 0.028% | Topical Analgesic |
| Menthol 4.574% | Topical Analgesic |
For external use only.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Keep away from heat. Store between 15° and 30° C (59° and 86° F).
diazoldinyl urea, ethyl alcohol, iodopropynyl butlylcarbamate, menthyl lactate, propylene glycol, sodium stearate, steareth-21, tetrasodium EDTA, triethenolamine, water
call 1-800-379-8870, Weekdays 9AM to 5PM EST or visit us online at activ-on.com
Dist. by Family First Pharmaceuticals, Inc., Reno, NV 89502
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