DECORTE AQ UV PROTECTION
- Product NDC
- 66820-0300
- 11-digit product format
- 668200300
- Labeler code
- 66820
- Product ID
- 66820-0300_ee3c4a33-e994-da48-e053-2995a90a09cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- titanium dioxide, zinc oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- KOSE AMERICA, INC.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-03-01
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 128 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66820-0300 | DECORTE AQ UV PROTECTION (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [KOSE AMERICA, INC.] | 3 | Legacy NDC | 20241020_c6bddc60-2a00-4405-9c4a-48626ee55eb4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66820-0300-1 | 66820030001 | 1 TUBE in 1 CARTON (66820-0300-1) > 50 mL in 1 TUBE | 1 tube | 2022-03-01 | 0000-00-00 | No | No | Current |
| 66820-0300-2 | 66820030002 | 5 mL in 1 TUBE (66820-0300-2) | 5 ml | 2022-03-01 | 0000-00-00 | No | No | Current |
| 66820-0300-3 | 66820030003 | .5 mL in 1 PACKET (66820-0300-3) | | 2022-03-01 | 0000-00-00 | No | No | Current |