Max Revive Plaster
- Product NDC
- 82198-0019
- Requested package NDC
- 82198-0019-1
- 11-digit product format
- 821980019
- Labeler code
- 82198
- Product ID
- 82198-0019_5e49325a-5938-0569-e063-6394a90a85c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol, Methyl Salicylate
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- Big 5 Nutrition LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-01
- Substance
- MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE
- Active strength
- .05; .01 g/g; g/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Max Revive Plaster
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | .05 g/g |
| METHYL SALICYLATE | .01 g/g |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82198-0019-1 | 82198001901 | 3 PATCH in 1 BAG (82198-0019-1) / 2.3 g in 1 PATCH | 3 patch | 2026-01-01 | No | No | Current |