Pain Relief Gel
- Product NDC
- 73672-989
- 11-digit product format
- 736720989
- Labeler code
- 73672
- Product ID
- 73672-989_bdc694d9-cc93-515d-e053-2a95a90aec0a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol 1.5%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- HEMPFUSION, INC.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-02-10
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 15 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 73672-989-50 | Pain Relief Gel | 1 in 1 CARTON | GEL | 1 | | 3 |
| 73672-989-50 | Pain Relief Gel | 50 mL in 1 BOTTLE | GEL | 50 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73672-989 | PAIN RELIEF GEL (MENTHOL 1.5%) GEL [HEMPFUSION, INC.] | 3 | Legacy NDC, 2 package rows | 20210319_bb270f7b-e5b6-41a4-e053-2995a90a559f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73672-989-50 | 73672098950 | 1 BOTTLE in 1 CARTON (73672-989-50) > 50 mL in 1 BOTTLE | 1 bottle | 2020-02-10 | 0000-00-00 | No | No | Current |