DynaRub
- Product NDC
- 67777-113
- 11-digit product format
- 677770113
- Labeler code
- 67777
- Product ID
- 67777-113_275e9d16-0717-f77a-e063-6394a90abb49
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pain Relieving Cream
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Dynarex Corporation
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-09-12
- Substance
- MENTHOL; METHYL SALICYLATE
- Active strength
- 10; 15 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DynaRub
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 10 g/100g |
| METHYL SALICYLATE | 15 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A, LAV5U5022Y |
| Rxcui | 311498 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67777-113-49 | DynaRub | 85 g in 1 TUBE | CREAM | 85 | | 3 |
| 67777-113-50 | DynaRub | 72 in 1 CASE | CREAM | 72 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67777-113 | DYNARUB (PAIN RELIEVING CREAM) CREAM [DYNAREX CORPORATION] | 3 | Current NDC, Legacy NDC, 2 package rows | 20241122_7f853941-a2d7-ed26-e053-2991aa0aa9ee.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 |
|---|
| 67777-113-49 | 67777011349 | 85 g in 1 TUBE | 85 g | | | | | Historical |
| 67777-113-50 | 67777011350 | 72 TUBE in 1 CASE (67777-113-50) / 85 g in 1 TUBE (67777-113-49) | 72 tube | 2016-09-12 | 0000-00-00 | No | No | Current |