Point Relief cold Spot Pain Relieving
- Product NDC
- 51452-038
- 11-digit product format
- 514520038
- Labeler code
- 51452
- Product ID
- 51452-038_85799c07-0b9e-20e5-e053-2a91aa0a4f0a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Fabrication Enterprises
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-04-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 100 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51452-038-01 | 51452003801 | 120 mL in 1 BOTTLE, SPRAY (51452-038-01) | 120 ml | 2019-04-01 | 0000-00-00 | No | No | Current |
| 51452-038-02 | 51452003802 | 475 mL in 1 BOTTLE, SPRAY (51452-038-02) | 475 ml | 2019-04-01 | 0000-00-00 | No | No | Current |