SMOOTH GATOR Head-Ezz Analgesic
- Product NDC
- 70673-501
- 11-digit product format
- 706730501
- Labeler code
- 70673
- Product ID
- 70673-501_1a820f59-518c-a238-e063-6294a90a1d1f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Smooth Gator LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-06-13
- Substance
- MENTHOL
- Active strength
- 30 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
- SMOOTH GATOR Head-Ezz Analgesic
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 30 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 1442261 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70673-501-00 | SMOOTH GATOR Head-Ezz Analgesic | 60 mL in 1 BOTTLE | CREAM | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70673-501 | SMOOTH GATOR HEAD-EZZ ANALGESIC (MENTHOL) CREAM [SMOOTH GATOR LLC] | 1 | Current NDC, 1 package rows | 20240613_02e18e5d-6fb0-4ebf-bdd6-dcc7edbb31bd.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 |
|---|
| 70673-501-00 | 70673050100 | 60 mL in 1 BOTTLE (70673-501-00) | 60 ml | 2024-06-13 | No | No | Historical |