Pain Relief Liquid Roller
- Product NDC
- 72562-167
- 11-digit product format
- 725620167
- Labeler code
- 72562
- Product ID
- 72562-167_29591578-c164-5ed4-e063-6394a90a7df3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Camphor 3.5%, Menthol 3.5%
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Tommie Copper, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-08-19
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL
- Active strength
- 3.5; 3.5 g/100g; 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
- Pain Relief Liquid Roller
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CAMPHOR (SYNTHETIC) | 3.5 g/100g |
| MENTHOL | 3.5 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5TJD82A1ET, L7T10EIP3A |
| Rxcui | 2467741 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72562-167-25 | Pain Relief Liquid Roller | 70 g in 1 BOTTLE, PLASTIC | LIQUID | 70 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72562-167 | PAIN RELIEF LIQUID ROLLER (CAMPHOR 3.5%, MENTHOL 3.5%) LIQUID [TOMMIE COPPER, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241217_c9f0447e-de43-16a5-e053-2995a90a05c1.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 |
|---|
| 72562-167-25 | 72562016725 | 70 g in 1 BOTTLE, PLASTIC (72562-167-25) | 70 g | 2021-08-19 | 0000-00-00 | No | No | Current |