Biofreeze Foam
- Product NDC
- 59316-991
- 11-digit product format
- 593160991
- Labeler code
- 59316
- Product ID
- 59316-991_51b59ff7-ac73-08c9-e063-6294a90aaa23
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Reckitt Benckiser LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-01-27
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 70 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Biofreeze Foam
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 70 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 2274104, 2274107 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59316-991-10 | Biofreeze Foam | 88 mL in 1 BOTTLE | LIQUID | 88 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59316-991 | BIOFREEZE FOAM (MENTHOL) LIQUID [RB HEALTH (US) LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241228_890191e8-99ad-489c-8f21-2592f3d31936.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 |
|---|
| 59316-991-10 | 59316099110 | 88 mL in 1 BOTTLE (59316-991-10) | 88 ml | 2020-01-27 | 0000-00-00 | No | No | Current |