HEB Tinted 30 Mineral Sunscreen For Face Lotion

HEB Tinted 30 Mineral Sunscreen For Face by

Drug Labeling and Warnings

HEB Tinted 30 Mineral Sunscreen For Face by is a Otc medication manufactured, distributed, or labeled by H.E.B.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HEB TINTED 30 MINERAL SUNSCREEN FOR FACE- titanium dioxide, zinc oxide lotion 
H.E.B.

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HEB Tinted 30 Mineral Sunscreen For Face Lotion

Active ingredients

Titanium Dioxide 3.33%, Zinc Oxide 3.5%

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

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

  • rash occurs

Keep out of reach of children.

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

Directions

apply liberally 15 minutes before sun exposure

reapply:

after 80 minutes of swimming or sweating

immediately after towel drying

at least every 2 hours

children under 6 months of age: 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 sunscreen 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 the product in this container from excessive heat and direct sun

may stain or damage some fabrics, materials or surfaces

Inactive ingredients

Water, Neopentyl Glycol Diheptanoate, Caprylic/Capric Triglyceride, Butyloctyl Salicylate, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Sorbitan Sesquioleate, C30-38 Olefin/Isopropyl Maleate/MA Copolymer, Sorbitan Tristearate, Stearyl/Octyldodecyl Citrate Crosspolymer, VP/Hexadecene Copolymer, Simmondsia Chinensis(jojoba) Seed Oil, Phenoxyethanol, Magnesium Sulfate, Silica, Maranta Arundinacea(Arrowroot) Root Extract, Ethylhexylglycerin, Glyceryl Stearate, Tocopherol, Sodium Phytate, Stearyl Alcohol, Cetyl Alcohol, Arachidyl Alcohol, Behenyl Alcohol, Arachidyl Glucoside, Polysorbate 60, Sodium Hydroxide, Iron Oxides.

Label

HEB56575A

HEB TINTED 30 MINERAL SUNSCREEN FOR FACE 
titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 37808-145
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE35 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE33.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)  
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
DOCOSANOL (UNII: 9G1OE216XY)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
JOJOBA OIL (UNII: 724GKU717M)  
HEXADECYL POVIDONE (UNII: AG75W62QYU)  
WATER (UNII: 059QF0KO0R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
PHYTATE SODIUM (UNII: 88496G1ERL)  
SORBITAN TRISTEARATE (UNII: 6LUM696811)  
GLYCERIN (UNII: PDC6A3C0OX)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
STEARYL/OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: PN88NW0KPK)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T)  
MARANTA ARUNDINACEA ROOT (UNII: FVN346W31A)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 37808-145-0989 mL in 1 TUBE; Type 0: Not a Combination Product01/28/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02001/28/202106/20/2024
Labeler - H.E.B. (007924756)

Revised: 10/2024

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