Land: USA
Språk: engelsk
Kilde: NLM (National Library of Medicine)
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51), OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)
NATURE REPUBLIC CO., LTD.
OCTINOXATE
OCTINOXATE 3.42 mg in 57 mL
TOPICAL
OTC DRUG
Purpose: Sunscreen [UV Protection] HOW TO USE: Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays.
OTC monograph not final
PROVENCE CALENDULA FRESH SUN- OCTINOXATE, OCTISALATE GEL NATURE REPUBLIC CO., LTD. _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 INGREDIENT Active Ingredient: ETHYLHEXYL METHOXYCINNAMATE 6.00%, ETHYLHEXYL SALICYLATE 3.00% INACTIVE INGREDIENT Inactive Ingredients: WATER, BUTYLENE GLYCOL, CYCLOPENTASILOXANE,ALCOHOL, ISOAMYL P-METHOXYCINNAMATE,DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE,1,2-HEXANEDIOL,TRIETHANOLAMINE,DIPROPYLENE GLYCOL,PEG/PPG-30/10 DIMETHICONE,SILICA,CARBOMER,VISCUM ALBUM (MISTLETOE) LEAF EXTRACT,CENTELLA ASIATICA EXTRACT,PORTULACA OLERACEA EXTRACT,CETETH- 10,FRAGRANCE,PHENOXYETHANOL,BEHENYL ALCOHOL,ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER,OCTYLDODECANOL,CALENDULA OFFICINALIS FLOWER EXTRACT,ECHIUM PLANTAGINEUM SEED OIL,SODIUM HYALURONATE,CARDIOSPERMUM HALICACABUM FLOWER/LEAF/VINE EXTRACT,HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLES PURPOSE Purpose: Sunscreen [UV Protection] CAUTIONS CAUTIONS: 1. For external use only. 2. Avoid contact with eyes and mouth. 3. Discontinue use if signs of irritation or rashes appear. 4. Keep out of reach of children. 5. Replace the cap after use. KEEP OUT OF REACH OF CHILDREN KEEP OUT OF REACH OF CHILDREN HOW TO USE HOW TO USE: Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays. PACKAGE LABEL.PRINCIPAL DISPLAY PANEL PROVENCE CALENDULA FRESH SUN octinoxate, octisalate gel PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:51346 -28 5 ROUTE OF ADMINISTRATION TOPICAL NATURE REPUBLIC CO., LTD. ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH O CTINO XATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 3.42 mg in 57 mL O CTISALATE (UNII: 4X49 Y0 59 6 W) (OCTISALATE - UNII:4X49 Y0 59 6 W) OCTISALATE 1.71 mg in 57 mL INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH WATER (UNII: 0 Les hele dokumentet