Pain Relief
- Product NDC
- 47682-321
- 11-digit product format
- 476820321
- Labeler code
- 47682
- Product ID
- 47682-321_3e4ee639-9aef-38c5-e063-6394a90a9ad3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Analgesic Menthol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Unifirst First Aid Corporation
- Application
- M015
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-04-01
- Substance
- MENTHOL
- Active strength
- 70 mg/L
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 70 mg/L |
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 |
|---|
| 47682-321-02 | Pain Relief | 0.059 L in 1 BOTTLE, SPRAY | SPRAY | 0.059 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 47682-321 | PAIN RELIEF (ANALGESIC MENTHOL) SPRAY [UNIFIRST FIRST AID CORPORATION] | 6 | Current NDC, Legacy NDC, 1 package rows | 20240117_8162d22d-04c0-de07-e053-2991aa0a9975.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 47682-321-02 | 47682032102 | .059 L in 1 BOTTLE, SPRAY (47682-321-02) | 2019-04-01 | 0000-00-00 | No | No | Current |