Biofreeze Professional
- Product NDC
- 68071-4325
- 11-digit product format
- 680714325
- Labeler code
- 68071
- Product ID
- 68071-4325_1a3dd23e-1c5a-9d41-e063-6394a90a3455
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, UNSPECIFIED FORM
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- M004
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-06-03
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 50 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
- Biofreeze Professional
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 415975, 1794892 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-4325-4 | Biofreeze Professional | 120 mL in 1 TUBE | GEL | 120 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-4325 | BIOFREEZE PROFESSIONAL (MENTHOL, UNSPECIFIED FORM) GEL [NUCARE PHARMACEUTICALS,INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20240608_66ff9726-20da-688a-e053-2a91aa0a59ac.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 |
|---|
| 68071-4325-4 | 68071432504 | 120 mL in 1 TUBE (68071-4325-4) | 120 ml | 2018-03-09 | 0000-00-00 | No | No | Current |