Biofreeze Colorless
- Product NDC
- 50090-6361
- 11-digit product format
- 500906361
- Labeler code
- 50090
- Product ID
- 50090-6361_d27f9f48-e60b-4599-a1d6-d243dfcabda5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-01-03
- Substance
- MENTHOL
- Active strength
- 40 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 Colorless
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 40 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 415974, 1111683 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6361-0 | Biofreeze Colorless | 89 mL in 1 BOTTLE | GEL | 89 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6361 | BIOFREEZE COLORLESS (MENTHOL) GEL [A-S MEDICATION SOLUTIONS] | 4 | Current NDC, 1 package rows | 20241113_cc1cba14-da40-4d7d-b522-b5c648798e96.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6361-0 | 50090636100 | 89 mL in 1 BOTTLE (50090-6361-0) | 89 ml | 2023-02-08 | No | No | Historical |