Laser Sunscreen 100
- Product NDC
- 76344-8001
- 11-digit product format
- 763448001
- Labeler code
- 76344
- Product ID
- 76344-8001_54dbdbc2-cda4-17cf-e054-00144ff8d46c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Humex,Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; ZINC OXIDE; TITANIUM DIOXIDE
- Active strength
- 8 g/100mL; g/100mL; g/100mL; g/100mL
- 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 |
|---|
| 76344-8001-2 | 76344800102 | 1 TUBE in 1 BOX (76344-8001-2) > 50 mL in 1 TUBE (76344-8001-1) | 1 tube | 2017-07-26 | 0000-00-00 | No | No | Current |