Dr. Ds Super 7 Pain Relief
- Product NDC
- 72246-112
- 11-digit product format
- 722460112
- Labeler code
- 72246
- Product ID
- 72246-112_b9e9ab5b-aff7-e8cf-e053-2995a90a93f5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- menthyl salicylate and menthol
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Promedx Innovations Inc
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-09-04
- Marketing end
- 0000-00-00
- Substance
- MENTHOL; MENTHYL SALICYLATE, (+/-)-
- Active strength
- 20 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72246-112 | DR. DS SUPER 7 PAIN RELIEF (MENTHYL SALICYLATE AND MENTHOL) CREAM [PROMEDX INNOVATIONS INC] | 2 | Legacy NDC | 20210129_aaca1fbf-aed6-4fe0-9821-6fa897b5d41e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72246-112-01 | 72246011201 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (72246-112-01) > 88 mL in 1 BOTTLE, WITH APPLICATOR | 2019-09-04 | 0000-00-00 | No | No | Current |