Vicks VapoRub
- Product NDC
- 37000-917
- 11-digit product format
- 370000917
- Labeler code
- 37000
- Product ID
- 37000-917_bb2663d5-6f3d-8a80-e053-2a95a90af111
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Camphor (synthetic), Eucalyptus oil, and Menthol
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-07-03
- Marketing end
- 0000-00-00
- Substance
- CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL
- Active strength
- 0 g/g; g/g; g/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37000-917-01 | 37000091701 | 1 JAR in 1 BLISTER PACK (37000-917-01) > 100 g in 1 JAR | 1 jar | 2018-07-03 | 0000-00-00 | No | No | Current |