Copperlife Pain Relief Liquid
- Product NDC
- 72562-121
- 11-digit product format
- 725620121
- Labeler code
- 72562
- Product ID
- 72562-121_295926bb-cc5a-4103-e063-6394a90a5ee7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol 16%
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Tommie Copper, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-08-10
- Substance
- MENTHOL
- Active strength
- 16 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
- Copperlife Pain Relief Liquid
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 16 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 |
|---|
| 72562-121-25 | Copperlife Pain Relief Liquid | 70 g in 1 BOTTLE, PLASTIC | SPRAY | 70 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72562-121 | COPPERLIFE PAIN RELIEF LIQUID (MENTHOL 16%) SPRAY [TOMMIE COPPER, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241217_c93a0139-953b-5523-e053-2a95a90a0b2d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72562-121-25 | 72562012125 | 70 g in 1 BOTTLE, PLASTIC (72562-121-25) | 70 g | 2021-08-10 | 0000-00-00 | No | No | Current |