HYDRA VIZOR HUEZ TINTED MOISTURIZER BROAD SPECTRUM SPF 30- zinc oxide lotion

HYDRA VIZOR HUEZ TINTED MOISTURIZER by

Drug Labeling and Warnings

HYDRA VIZOR HUEZ TINTED MOISTURIZER by is a Otc medication manufactured, distributed, or labeled by KENDO HOLDINGS INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ZINC OXIDE 15.5%

PURPOSE

SUNSCREEN

USES

HELPS PREVENT SUNBURN
IF USED AS DIRECTED WITH OTHER SUN PROTECTION MEASURES (SEE DIRECTIONS), DECREASES THE RISK OF SKIN CANCER AND EARLY SKIN AGING CAUSED BY THE SUN.

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.

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

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

PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN.

INACTIVE INGREDIENTS

WATER, C12-15 ALKYL BENZOATE, CAPRYLIC/CAPRIC TRIGLYCERIDE, C15-19 ALKANE, BUTYLOCTYL SALICYLATE, PHENYL TRIMETHICONE, GLYCERYL CITRATE/LACTATE/LINOLEATE/OLEATE, DIMETHICONE, SORBITAN ISOSTEARATE, ETHYLHEXYL PALMITATE, BUTYLENE GLYCOL, QUATERNIUM-90 BENTONITE, POLYHYDROXYSTEARIC ACID, NIACINAMIDE, 1,2-HEXANEDIOL, ADANSONIA DIGITATA PULP EXTRACT, ALOE BARBADENSIS LEAF JUICE, BAROSMA BETULINA LEAF EXTRACT, CAPRYLYL GLYCOL, CAPRYLYL/CAPRYL GLUCOSIDE, CETYL ALCOHOL, CITRIC ACID, CITRULLUS LANATUS (WATERMELON) SEED EXTRACT, DISTEARDIMONIUM HECTORITE, ETHYLHEXYLGLYCERIN, GLYCERIN, GLYCERYL STEARATE SE, HYALURONIC ACID, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, ISOPROPYL TITANIUM TRIISOSTEARATE, PHENOXYETHANOL, POLYISOBUTENE, POLYSILICONE-11, POTASSIUM SORBATE, SILICA, SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, SODIUM BENZOATE, SODIUM HYALURONATE, SORBITAN OLEATE, TOCOPHEROL, TOCOPHERYL ACETATE, TRIETHYL CITRATE, XANTHAN GUM. MAY CONTAIN (+/-): IRON OXIDES,TITANIUM DIOXIDE.

QUESTIONS?

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HYDRA VIZOR HUEZ TINTED MOISTURIZER  BROAD SPECTRUM SPF 30
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71499-083
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
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
CETYL ALCOHOL (UNII: 936JST6JCN)
WATERMELON SEED (UNII: N364973Y9Q)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
GLYCERYL CITRATE/LACTATE/LINOLEATE/OLEATE (UNII: A5SAE9KW2M)
HYALURONIC ACID (UNII: S270N0TRQY)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
XANTHAN GUM (UNII: TTV12P4NEE)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
C15-19 ALKANE (UNII: CI87N1IM01)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
QUATERNIUM-90 BENTONITE (UNII: 97K5YEF88C)
NIACINAMIDE (UNII: 25X51I8RD4)
ADANSONIA DIGITATA FRUIT PULP (UNII: P65OHK3GHP)
BROWN IRON OXIDE (UNII: 1N032N7MFO)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
POLYISOBUTYLENE (1300 MW) (UNII: 241BN7J12Y)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
AGATHOSMA BETULINA LEAF (UNII: 369DDH39Z0)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
DIMETHICONE 20 (UNII: H8YMB5QY0D)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71499-083-01	1 in 1 BOX	05/24/2024
1		50 mL in 1 BOTTLE, PUMP; 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	05/24/2024

Labeler - KENDO HOLDINGS INC. (078489982)

Registrant - KENDO HOLDINGS INC. (078489982)