aKwa Daystar Shade
- Manufacturer
- Northwest Cosmetic Laboratories, LLC dba Elevation Labs, Idaho
- Effective date
- 2022-06-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:59:52
Label at a glance#
ProductaKwa Daystar Shade SPF 40
Active ingredientHOMOSALATE, zinc oxide, OCTISALATE
Label structure1 sections
Label contents#
Full prescribing information#
Products#
Every source-derived product name is available through these pages.
- aKwa Daystar Shade SPF 40
- Homosalate, Zinc Oxide, Octisalate
- HOMOSALATE
- zinc oxide
- ZINC CATION
- OCTISALATE
- WATER
- BUTYLOCTYL SALICYLATE
- COCO-CAPRYLATE/CAPRATE
- GLYCERIN
- GLYCERYL STEARATE SE
- PEG-100 STEARATE
- DIMETHICONE
- C14-22 ALCOHOLS
- ISODODECANE
- MEDIUM-CHAIN TRIGLYCERIDES
- ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%)
- PHENYL TRIMETHICONE
- TRIBASIC CALCIUM PHOSPHATE
- CAPRYLYL GLYCOL
- BENZYL ALCOHOL
- CETEARYL GLUCOSIDE
- VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER
- POLYGLYCERYL-3 RICINOLEATE
- C12-20 ALKYL GLUCOSIDE
- DISTEARDIMONIUM HECTORITE
- ISOSTEARIC ACID
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
- BENZOIC ACID
- XANTHAN GUM
- LINOLEIC ACID
- EGG PHOSPHOLIPIDS
- PROPYLENE CARBONATE
- EDETATE DISODIUM
- .ALPHA.-TOCOPHEROL ACETATE
- CANOLA OIL
- TETRAHEXYLDECYL ASCORBATE
- OLEIC ACID
- PALMITIC ACID
- 1,2-HEXANEDIOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62282-410 | 62282-410-01, 62282-410-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 14fbd002-6392-4408-88bd-ff937a6d14ea | f2717c35-2c82-4cc0-a53d-d47d3efce11b | 2022-06-06 | 14fbd002-6392-4408-88bd-ff937a6d14ea f2717c35-2c82-4cc0-a53d-d47d3efce11b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
