Label: FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 SUNSCREEN MOISTURIZER- zinc oxide cream
- NDC Code(s): 71499-135-01
- Packager: KENDO HOLDINGS INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 7, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
-
DIRECTIONS
- APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.
- USE A WATER RESISTANT SUNSCREEN IF SWIMMING OR SWEATING.
- REAPPLY AT LEAST EVERY 2 HOURS.
- CHILDREN UNDER 6 MONTHS: ASK A DOCTOR.
- SUN PROTECTION MEASURES. SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY SKIN AGING. TO DECREASE THIS RISK, REGULARLY USE A SUNCREEN WITH A BROAD SPECTRUM SPF VALUE OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDING:
- LIMIT TIME IN THE SUN, ESPECIALLY FROM 10 A.M. - 2 P.M.
- WEAR LONG=SLEEVED SHIRTS, PANTS, HATS, AND SUNGLASSES.
- OTHER INFORMATION
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INACTIVE INGREDIENTS
WATER, C12-15 ALKYL BENZOATE, CAPRYLIC/CAPRIC TRIGLYCERIDES, BUTYLOCTYL SALICYLATE, DIMETHICONE, GLYCERIN, ETHYLHEXYL PALMITATE, PROPANEDIOL, BUTYROSPREMUM PARKII (SHEA) BUTTER, CARTHAMUS TINCTORIUS (SAFFLOWER) .SEED OLEOSOMES, GLYCERYL STEARATE SE, BUTYLENE GLYCOL, POLYHYDROXYSTEARIC ACID, SORBITAN ISOSTEARATE, CETYL ALCOHOL, NIACINAMIDE, PENTAERYTHRITYL TETRAISOSTEARATE, PHENYL TRIMETHICONE, SILICA, HYALURONIC ACID, SODIUM HYALURONATE, CITRULLUS LANATUS (WATERMELON) SEED EXTRACT, ADANSONIA DIGITATA PULP EXTRACT, BAROSMA BETULINA LEAF EXTRACT, ALOE BARBADENSIS LEAF JUICE, TOCOPHEROL, GLUCONOLACTONE, INULIN LAURYL CARBAMATE, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, XANTHAN GUM, HYDROXYACETOPHENONE, POLYSILICONE-11, TRISODIUM ETHYLENEDIAMINE DISUCCINATE, SODIUM CITRATE, CITRIC ACID, BENZYL SALICYLATE, ETHYLHEXYLGLYCERIN, SODIUM BENZOATE, POTASSIUM SORBATE, PHENOXYETHANOL, FRAGRANCE, HEXYL CINNAMAL, LIMONENE, LINALOOL, YELLOW 6, RED 33.
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INGREDIENTS AND APPEARANCE
FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 SUNSCREEN MOISTURIZER
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71499-135 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 15.5 g in 100 mL Inactive Ingredients Ingredient Name Strength POTASSIUM SORBATE (UNII: 1VPU26JZZ4) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) SODIUM BENZOATE (UNII: OJ245FE5EU) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) DIMETHICONE (UNII: 92RU3N3Y1O) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) SHEA BUTTER (UNII: K49155WL9Y) NIACINAMIDE (UNII: 25X51I8RD4) HYALURONIC ACID (UNII: S270N0TRQY) HYALURONATE SODIUM (UNII: YSE9PPT4TH) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYL PALMITATE (UNII: 2865993309) PROPANEDIOL (UNII: 5965N8W85T) CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) TOCOPHEROL (UNII: R0ZB2556P8) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) CETYL ALCOHOL (UNII: 936JST6JCN) PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) WATERMELON SEED (UNII: N364973Y9Q) ADANSONIA DIGITATA FRUIT PULP (UNII: P65OHK3GHP) AGATHOSMA BETULINA LEAF (UNII: 369DDH39Z0) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLUCONOLACTONE (UNII: WQ29KQ9POT) INULIN LAURYL CARBAMATE (UNII: 48RFF58ESG) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) XANTHAN GUM (UNII: TTV12P4NEE) D&C RED NO. 33 (UNII: 9DBA0SBB0L) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) LIMONENE, (+)- (UNII: GFD7C86Q1W) LINALOOL, (+/-)- (UNII: D81QY6I88E) BENZYL SALICYLATE (UNII: WAO5MNK9TU) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71499-135-01 1 in 1 BOX 06/01/2023 1 50 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/01/2023 Labeler - KENDO HOLDINGS INC (078489982)