SUNSCREEN- octinoxate, octisalate, zinc oxide gel 
HEB

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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Broad Spectrum SPF 50
726.001/726AA

claims

H-E-B

Solutions

sunscreen

Active ingredient

Octinoxate 7.5%

Octisalate 5%

Zinc oxide 10%

Purpose

Sunscreen

Use

Warnings

For external use only

Do not use

When using this product

Stop use and ask a doctor if

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

other information

inactive ingredients

water, butyloctyl salicylate, C12-15 alkyl benzoate, caprylic/capric triglyceride, glyceryl stearate, propanediol, triacontanyl PVP, cetearyl alcohol, PEG-100 stearate, cetearyl glucoside, glyceryl behenate, dimethicone, glycerin, PEG-150/decyl alcohol/SMDI copolymer, Aloe barbadensis leaf juice, allantoin, panthenol, tocopheryl acetate, triethoxycaprylylsilane, fragrance, phenoxyethanol, methylisothiazolinone, tetrasodium EDTA

Questions?

1-800-527-7731

Disclaimer

May stain or damage some fabrics or surfaces

MADE WITH PRIDE AND CARE FOR H-E-B

SAN ANTONIO, TN 78204

MADE IN USA WITH U.S AND FOREIGN PARTS

100% GUARANTEE

Promise

If you aren't completely pleased with this product, we'll be happy to replace it or refund your money.  You have our word on it

Principal panel display

H-E-B

Solutions

Sunscreen

CLEAR

ZINC

WITH OCTINOXATE & OCTISALATE

SUNSCREEN

BROAD SPECTRUM SPF 50

SPF 50

FOR FACE, NOSE OR EARS

NET WT.

1 OZ (28.3 g)

image description

SUNSCREEN 
octinoxate, octisalate, zinc oxide gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-726
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE562 g  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE250 g  in 1 g
Zinc oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION1000 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PROPANEDIOL (UNII: 5965N8W85T)  
TRICONTANYL POVIDONE (UNII: N0SS3Q238D)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
PEG-100 STEARATE (UNII: YD01N1999R)  
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
GLYCERYL BEHENATE/EICOSADIOATE (UNII: 73CJJ317SR)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERIN (UNII: PDC6A3C0OX)  
PEG-150/DECYL ALCOHOL/SMDI COPOLYMER (1350 MPA.S AT 3%) (UNII: VP5LS3541F)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ALLANTOIN (UNII: 344S277G0Z)  
PANTHENOL (UNII: WV9CM0O67Z)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
EDETATE SODIUM (UNII: MP1J8420LU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-726-1028.3 g in 1 PACKAGE; Type 0: Not a Combination Product06/06/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35206/06/2017
Labeler - HEB (007924756)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(37808-726)

Revised: 12/2022
Document Id: 88331672-bf21-4a69-b082-c8be601d4298
Set id: 858ac80c-a0e5-4f0a-aa9f-62698fb29f58
Version: 13
Effective Time: 20221209
 
HEB