SUNMED pain freeze
- Product NDC
- 73240-904
- 11-digit product format
- 732400904
- Labeler code
- 73240
- Product ID
- 73240-904_3cbd785f-2ab1-56e2-e063-6294a90a65fc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Sunflora Inc.
- Application
- M017.10
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-19
- Substance
- MENTHOL
- Active strength
- 6 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SUNMED pain freeze
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 6 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73240-904-01 | SUNMED pain freeze | 89 mL in 1 BOTTLE, PLASTIC | SPRAY | 89 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73240-904 | SUNMED PAIN FREEZE (MENTHOL) SPRAY [SUNFLORA INC.] | 1 | Current NDC, 1 package rows | 20230712_ff49699c-ced9-13d2-e053-6394a90af079.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 73240-904-01 | 73240090401 | 89 mL in 1 BOTTLE, PLASTIC (73240-904-01) | 89 ml | 2025-08-19 | No | No | Historical |