Pharmacys Prescription Vapor Rub
- Product NDC
- 72197-007
- 11-digit product format
- 721970007
- Labeler code
- 72197
- Product ID
- 72197-007_2c69c634-e137-1428-e063-6294a90aa8f1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- American Consumer Products Corp
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-09-28
- Substance
- CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL, UNSPECIFIED FORM
- Active strength
- 4.7; 1; 1 g/100g; 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
- Pharmacys Prescription Vapor Rub
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CAMPHOR (SYNTHETIC) | 4.7 g/100g |
| EUCALYPTUS OIL | 1 g/100g |
| MENTHOL, UNSPECIFIED FORM | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5TJD82A1ET, 2R04ONI662, L7T10EIP3A |
| Rxcui | 1042788 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72197-007-04 | Pharmacys Prescription Vapor Rub | 110 g in 1 BOTTLE, PLASTIC | GEL | 110 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72197-007 | PHARMACYS PRESCRIPTION VAPOR RUB (MENTHOL) GEL [AMERICAN CONSUMER PRODUCTS CORP] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250125_6ef328ff-f5c3-515d-e053-2a91aa0a32d3.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 |
|---|
| 72197-007-04 | 72197000704 | 110 g in 1 BOTTLE, PLASTIC (72197-007-04) | 110 g | 2018-09-28 | 0000-00-00 | No | No | Current |