Pharmacys Prescription Vapor Rub
- Product NDC
- 72197-046
- 11-digit product format
- 721970046
- Labeler code
- 72197
- Product ID
- 72197-046_31aa4b96-eb44-f42a-e063-6294a90ac37a
- 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
- 2021-02-09
- Substance
- CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL, UNSPECIFIED FORM
- Active strength
- 4.7; 1.2; 1.25 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 | 1.2 g/100g |
| MENTHOL, UNSPECIFIED FORM | 1.25 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5TJD82A1ET, 2R04ONI662, L7T10EIP3A |
| Rxcui | 2045202 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72197-046-04 | Pharmacys Prescription Vapor Rub | 110 g in 1 BOTTLE, PLASTIC | GEL | 110 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72197-046 | PHARMACYS PRESCRIPTION VAPOR RUB (MENTHOL) GEL [AMERICAN CONSUMER PRODUCTS CORP] | 1 | Current NDC, 1 package rows | 20250403_31aa54d8-df8d-f1ae-e063-6294a90a9622.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 |
|---|
| 72197-046-04 | 72197004604 | 110 g in 1 BOTTLE, PLASTIC (72197-046-04) | 110 g | 2025-03-31 | No | No | Current |