Biofreeze Roll-On
- Product NDC
- 50090-6358
- 11-digit product format
- 500906358
- Labeler code
- 50090
- Product ID
- 50090-6358_1e426c73-8145-47fe-9470-39c853f54446
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2013-01-17
- Substance
- MENTHOL
- Active strength
- 40 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6358-0 | Biofreeze Roll-On | 74 mL in 1 BOTTLE | GEL | 74 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6358 | BIOFREEZE ROLL-ON (MENTHOL) GEL [A-S MEDICATION SOLUTIONS] | 3 | Current NDC, 1 package rows | 20231102_814b37ea-5441-4cec-8794-71ca01d849ae.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 |
|---|
| 50090-6358-0 | 50090635800 | 74 mL in 1 BOTTLE (50090-6358-0) | 74 ml | 2023-02-07 | No | No | Historical |