Biofreeze Foot Pain Relief Set
- Product NDC
- 59316-002
- 11-digit product format
- 593160002
- Labeler code
- 59316
- Product ID
- 59316-002_51b58d16-badb-06b8-e063-6294a90a94ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- KIT
- Labeler
- Reckitt Benckiser LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-03-12
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Biofreeze Foot Pain Relief Set
- Listing expiration
- 2027-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 253020, 2001133 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59316-001-10 | Biofreeze Foot Pain Relief Set | 85 g in 1 TUBE | CREAM | 85 g | 100 mg in 1g | 6 |
| 59316-002-10 | Biofreeze Foot Pain Relief Set | 1 in 1 KIT | KIT | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59316-002 | BIOFREEZE FOOT PAIN RELIEF SET (MENTHOL) KIT [RB HEALTH (US) LLC] | 5 | Current NDC, Legacy NDC, 2 package rows | 20241228_4a885eef-0364-4655-bccc-7158c76cc5b2.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 |
|---|
| 59316-001-10 | 59316000110 | 85 g in 1 TUBE | 85 g | | | | | Historical |
| 59316-002-10 | 59316000210 | 1 KIT in 1 KIT (59316-002-10) * 85 g in 1 TUBE (59316-001-10) | 1 kit | 2021-03-12 | 0000-00-00 | No | No | Current |