HEMPCIN Advanced Topical Pain Relief Cream
- Product NDC
- 51151-391
- 11-digit product format
- 511510391
- Labeler code
- 51151
- Product ID
- 51151-391_0973b73d-5dd0-0986-e063-6294a90a5917
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Pedicis Research, LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-02-13
- Substance
- MENTHOL
- Active strength
- 50 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- HEMPCIN Advanced Topical Pain Relief Cream
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 50 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51151-391-00 | HEMPCIN Advanced Topical Pain Relief Cream | 60 g in 1 TUBE | CREAM | 60 | | 2 |
| 51151-391-00 | HEMPCIN Advanced Topical Pain Relief Cream | 1 in 1 BOX | CREAM | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51151-391 | HEMPCIN ADVANCED TOPICAL PAIN RELIEF CREAM (MENTHOL) CREAM [PEDICIS RESEARCH, LLC] | 2 | Current NDC, 2 package rows | 20231106_97f5e300-b780-4694-a681-60d5e0cfad65.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51151-391-00 | 51151039100 | 1 TUBE in 1 BOX (51151-391-00) / 60 g in 1 TUBE | 1 tube | 2023-02-13 | No | No | Current |