Cell Fusion C Laser Sunscreen
- Product NDC
- 52554-1200
- 11-digit product format
- 525541200
- Labeler code
- 52554
- Product ID
- 52554-1200_acba6f21-f1ca-48e0-923e-e284327df1cc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE, HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- CMS LAB Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-01
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE; HOMOSALATE; OCTISALATE; TITANIUM DIOXIDE
- Active strength
- 13 g/100mL; g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52554-1200-1 | 52554120001 | 10 mL in 1 CARTON (52554-1200-1) | 10 ml | 2020-05-01 | 0000-00-00 | No | No | Current |
| 52554-1200-2 | 52554120002 | 50 mL in 1 CARTON (52554-1200-2) | 50 ml | 2020-05-01 | 0000-00-00 | No | No | Current |