FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 SUNSCREEN MOISTURIZER- zinc oxide cream 
KENDO HOLDINGS INC

----------

KENDO - FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 MOISTURIZER (71499-135)

ACTIVE INGREDIENTS

ZINC OXIDE 15.5%

PURPOSE

SUNSCREEN

USES

WARNINGS

FOR EXTERNAL USE ONLY.

DO NOT USE ON DAMAGED OR BROKEN SKIN.

STOP USE AND ASK A DOCTOR IF RASH OCCURS.

WHEN USING THIS PRODUCT KEEP OUT OF EYES. RINSE WITH WATER TO REMOVE.

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

OTHER INFORMATION

PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN.

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.

QUESTIONS?

FENTYSKIN.COM

PDP

DF

FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 SUNSCREEN MOISTURIZER 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71499-135
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE15.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71499-135-011 in 1 BOX06/01/2023
150 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:71499-135-021 in 1 BOX06/01/2023
230 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02006/01/2023
Labeler - KENDO HOLDINGS INC (078489982)

Revised: 5/2024
Document Id: 19149a22-828a-be7b-e063-6394a90afb47
Set id: fd16def1-4c88-3ad0-e053-6294a90ab088
Version: 3
Effective Time: 20240522
 
KENDO HOLDINGS INC