FENTY SKIN HYDRA VIZOR  SPF 30- avobenzone, homosalate, octisalate lotion 
KENDO HOLDINGS INC

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.

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KENDO - FENTY SKIN HYDRA VIZOR - SPF 30 (71499-220)

ACTIVE INGREDIENTS

AVOBENZONE  3%

HOMOSALATE  9%

OCTISALATE  4.5%

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, GLYCERIN, CARTHAMUS TINCTORIUS SEED OLEOSOMES, PENTYLENE GLYCOL, BUTYLENE GLYCOL, C12-15 ALKYL BENZOATE, NIACINAMIDE, ZEA MAYS (CORN) STARCH, HYALURONIC ACID, SODIUM HYALURONATE, CITRULLUS LANATUS (WATERMELON) SEED EXTRACT, ADANSONIA DIGITATA PULP EXTRACT, BAROSMA BETULINA LEAF EXTRACT, ALOE BARBADENSIS LEAF JUICE, TOCOPHERYL ACETATE, GLUCONOLACTONE, SORBITAN OLEATE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER, DIMETHICONE, ISOHEXADECANE, ETHYLHEXYL METHOXYCRYLENE, POLYSORBATE 80, XANTHAN GUM, SODIUM HYDROXIDE, CITRIC ACID, POTASSIUM HYDROXIDE, TOCOPHEROL, TRISODIUM ETHYLENEDIAMINE DISUCCINATE, ETHYLHEXYLGLYCERIN, SODIUM BENZOATE, POTASSIUM SORBATE, PHENOXYETHANOL, FRAGRANCE, BENZYL SALICYLATE, CITRAL, HEXYL CINNAMAL, LIMONENE, LINALOOL, RED 33.

QUESTIONS?

FENTYSKIN.COM

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FENTY SKIN HYDRA VIZOR   SPF 30
avobenzone, homosalate, octisalate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71499-220
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE9 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
NIACINAMIDE (UNII: 25X51I8RD4)  
STARCH, CORN (UNII: O8232NY3SJ)  
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
AGATHOSMA BETULINA LEAF (UNII: 369DDH39Z0)  
WATERMELON SEED (UNII: N364973Y9Q)  
ADANSONIA DIGITATA FRUIT PULP (UNII: P65OHK3GHP)  
HYALURONIC ACID (UNII: S270N0TRQY)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
TOCOPHEROL (UNII: R0ZB2556P8)  
BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
CITRAL (UNII: T7EU0O9VPP)  
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71499-220-017 mL in 1 TUBE; Type 0: Not a Combination Product08/23/2020
2NDC:71499-220-0230 mL in 1 TUBE; Type 0: Not a Combination Product08/23/2020
3NDC:71499-220-0350 mL in 1 BOTTLE; Type 0: Not a Combination Product08/23/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35208/23/2020
Labeler - KENDO HOLDINGS INC (078489982)
Establishment
NameAddressID/FEIBusiness Operations
Englewood Lab, Inc.080987545manufacture(71499-220)

Revised: 1/2022
Document Id: d57c00cc-1583-5307-e053-2995a90abd36
Set id: 1d26bfb0-3c05-4a0c-9d4b-810359222730
Version: 4
Effective Time: 20220113
 
KENDO HOLDINGS INC