biochemistry PAIN RELIEF FOOT ACTIVE
- Product NDC
- 65121-209
- 11-digit product format
- 651210209
- Labeler code
- 65121
- Product ID
- 65121-209_482e2384-ef5c-01c7-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Pure Source, LLC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-02-06
- Marketing end
- 0000-00-00
- Substance
- BENZYL ALCOHOL; LIDOCAINE HYDROCHLORIDE
- Active strength
- 190 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 65121-209-31 | 65121020931 | 1 BOTTLE, SPRAY in 1 CARTON (65121-209-31) > 30 mL in 1 BOTTLE, SPRAY | 2017-02-09 | 0000-00-00 | No | No | Current |
| 65121-209-32 | 65121020932 | 1 BOTTLE, SPRAY in 1 CARTON (65121-209-32) > 60 mL in 1 BOTTLE, SPRAY | 2017-02-09 | 0000-00-00 | No | No | Current |