aKwa Daystar Shade
- Product NDC
- 62282-410
- Requested package NDC
- 62282-410-02
- 11-digit product format
- 622820410
- Labeler code
- 62282
- Product ID
- 62282-410_14fbd002-6392-4408-88bd-ff937a6d14ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Homosalate, Zinc Oxide, Octisalate
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Northwest Cosmetic Laboratories, LLC dba Elevation Labs, Idaho
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-06-02
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; OCTISALATE; ZINC OXIDE
- Active strength
- 10 g/100mL; g/100mL; g/100mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- 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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 62282-410-02 | 62282041002 | 1 TUBE in 1 CARTON (62282-410-02) > 60 mL in 1 TUBE (62282-410-01) | 1 tube | 2020-06-02 | 0000-00-00 | No | No | Current |