Daily SPF Facial SunscreenLotion Broad Spectrum SPF 32
- Product NDC
- 62742-4192
- 11-digit product format
- 627424192
- Labeler code
- 62742
- Product ID
- 62742-4192_a09f6a61-08e1-4e5c-9562-cf6eb866e85b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Allure Labs Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-11-03
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 210 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 62742-4192-2 | 62742419202 | 1 TUBE in 1 CARTON (62742-4192-2) > 48 g in 1 TUBE (62742-4192-1) | 1 tube | 2020-11-03 | 0000-00-00 | No | No | Current |