GOLDKIWI SUN SPF 36 PA PLUS PLUS
Dosage form: cream
Ingredients: OCTINOXATE 3.5g in 50g, TITANIUM DIOXIDE 2.05g in 50g, ZINC OXIDE 1.42g in 50g
Labeler: SKINFOOD CO., LTD.
NDC Code: 76214-034
Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Active ingredients: OCTINOXATE 7%, TITANIUM DIOXIDE 4.1%, ZINC OXIDE 2.85%
Inactive ingredients:
WATER, CYCLOPENTASILOXANE, ISOAMYL p-METHOXYCINNAMATE, CETYL PEG/PPG-10/1 DIMETHICONE, ACTINIDIA CHINENSIS (KIWI) FRUIT EXTRACT, SQUALANE, PROPYLENE GLYCOL, SODIUM CHLORIDE, SORBITAN SESQUIOLEATE, STEARALKONIUM HECTORITE, GLYCERIN, PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, PEG-10 DIMETHICONE, OZOKERITE, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TRIETHOXYCAPRYLYLSILANE, ALUMINUM HYDROXIDE, STEARIC ACID, DIMETHICONE/METHICONE COPOLYMER, POLYMETHYL METHACRYLATE, TRIETHANOLAMINE, CITRULLUS VULGARIS (WATERMELON) FRUIT EXTRACT, PRUNUS MUME FRUIT EXTRACT, SODIUM PALMITOYL PROLINE, NYMPHAEA ALBA FLOWER EXTRACT, PANTHENOL, DISODIUM COCOAMPHODIACETATE, TRITICUM VULGARE (WHEAT) GERM EXTRACT, SACCHAROMYCES CEREVISIAE EXTRACT, SODIUM HYALURONATE, PROPYLPARABEN, METHYLPARABEN, PHENOXYETHANOL, FRAGRANCE, SILICA
Purpose: Protects skin from UV rays.
Warnings:
For external use only.
Avoid contact with eyes.
Discontinue use if signs of irritation appear.
Keep out of reach of children:
Keep out of reach of children.
Indication and usage:
At the end of basic cosmetic care, apply in an adequate amount to body parts sensitive to UV radiation such as face, arms and legs, avoiding the eye area.
Dosage and administration:
For best results, apply at least 15 to 20 minutes before sun exposure.
Reapply frequently while out in the sun.
| GOLDKIWI SUN
SPF 36 PA PLUS PLUS
octinoxate cream |
||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Labeler - SKINFOOD CO., LTD. (690324173) |
| Registrant - SKINFOOD CO., LTD. (690324173) |
| Establishment | |||
| Name | Address | ID/FEI | Operations |
| SKINFOOD CO., LTD. | 690324173 | manufacture | |
Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.



