Ultra Strength Pain Relief Gel
- Product NDC
- 73287-023
- 11-digit product format
- 732870023
- Labeler code
- 73287
- Product ID
- 73287-023_275b89dc-566d-3bc1-e063-6394a90a9cad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- TELEBRANDS CORP
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-02-28
- Substance
- MENTHOL
- Active strength
- 8 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ultra Strength Pain Relief Gel
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 8 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73287-023-01 | Ultra Strength Pain Relief Gel | 1 in 1 CARTON | LOTION | 1 | | 2 |
| 73287-023-01 | Ultra Strength Pain Relief Gel | 71 g in 1 APPLICATOR | LOTION | 71 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73287-023 | ULTRA STRENGTH PAIN RELIEF GEL (MENTHOL) LOTION [TELEBRANDS CORP] | 2 | Current NDC, Legacy NDC, 2 package rows | 20241122_d91b2e09-550e-4968-e053-2995a90ae323.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73287-023-01 | 73287002301 | 1 APPLICATOR in 1 CARTON (73287-023-01) / 71 g in 1 APPLICATOR | 1 applicator | 2022-02-28 | 0000-00-00 | No | No | Current |