Flexible Pain Relief Roll-on Extra Strength
- Product NDC
- 73096-030
- 11-digit product format
- 730960030
- Labeler code
- 73096
- Product ID
- 73096-030_d4791ad7-c058-f925-e053-2995a90a9f78
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pain Relief Roll-on Extra Strength
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- ABACUS HEALTH PRODUCTS, INC.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-07-10
- Marketing end
- 0000-00-00
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 2126 mg/85.05g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73096-030-02 | 73096003002 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (73096-030-02) > 85.05 g in 1 BOTTLE, WITH APPLICATOR (73096-030-01) | 2019-07-10 | 0000-00-00 | No | No | Current |