NEUROFLEX Topical Pain Relieving Liquid
- Product NDC
- 69876-1740
- 11-digit product format
- 698761740
- Labeler code
- 69876
- Product ID
- 69876-1740_09d72589-142c-349f-e063-6294a90a4d95
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CAMPHOR (SYNTHETIC), MENTHOL
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Almark Products Inc
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-04-01
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL
- Active strength
- 30; 20 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- NEUROFLEX Topical Pain Relieving Liquid
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CAMPHOR (SYNTHETIC) | 30 mg/mL |
| MENTHOL | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5TJD82A1ET, L7T10EIP3A |
| Rxcui | 2534165 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69876-1740-0 | NEUROFLEX Topical Pain Relieving Liquid | 118 mL in 1 BOTTLE, SPRAY | SOLUTION | 118 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69876-1740 | NEUROFLEX TOPICAL PAIN RELIEVING LIQUID (CAMPHOR (SYNTHETIC), MENTHOL) SOLUTION [ALMARK PRODUCTS INC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231111_6da3aa84-7a01-4041-8792-a4bbf49e6e4e.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 |
|---|
| 69876-1740-0 | 69876174000 | 118 mL in 1 BOTTLE, SPRAY (69876-1740-0) | 118 ml | 2021-04-01 | 0000-00-00 | No | No | Current |