ARNIMAX Penetrating Pain Relief Gel
- Product NDC
- 35324-274
- 11-digit product format
- 353240274
- Labeler code
- 35324
- Product ID
- 35324-274_09d7163b-7e66-1473-e063-6294a90a81a1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- WYNNPHARM INC.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-02-15
- Substance
- MENTHOL
- Active strength
- 30 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ARNIMAX Penetrating Pain Relief Gel
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 30 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 259150 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 35324-274-00 | ARNIMAX Penetrating Pain Relief Gel | 75 g in 1 TUBE | GEL | 75 | | 2 |
| 35324-274-00 | ARNIMAX Penetrating Pain Relief Gel | 1 in 1 BOX | GEL | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 35324-274 | ARNIMAX PENETRATING PAIN RELIEF GEL (MENTHOL) GEL [WYNNPHARM INC.] | 2 | Current NDC, Legacy NDC, 2 package rows | 20231111_3a31f805-19c6-4036-a663-ebef9b212007.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35324-274-00 | 35324027400 | 1 TUBE in 1 BOX (35324-274-00) / 75 g in 1 TUBE | 1 tube | 2022-02-15 | 0000-00-00 | No | No | Current |