HEB FACE 50 CLEAR ZINC SUNSCREEN- octocrylene, zinc oxide lotion

HEB Face 50 Clear Zinc Sunscreen by

Drug Labeling and Warnings

HEB Face 50 Clear Zinc Sunscreen by is a Otc medication manufactured, distributed, or labeled by H.E.B.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Octocrylene 4.0%, Zinc Oxide 5.0%

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, Ethylhexyl Stearate, Diisopropyl Adipate, Cetyl Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Hydrogenated Castor Oil, Polyglyceryl-4 Isostearate, Hexyl Laurate, Beeswax, Isohexadecane, Silica, Ethylhexylglycerin, Chlorphenesin, Fragrance, Triethoxycaprylylsilane, Dimethicone, Sodium Chloride, Aloe Barbadensis Leaf Juice, Sodium Ascorbyl Phosphate, Tocopherol.

Label

INGREDIENTS AND APPEARANCE

HEB FACE 50 CLEAR ZINC SUNSCREEN 
octocrylene, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-151
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	50 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	40 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
ISOHEXADECANE (UNII: 918X1OUF1E)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HEXYL LAURATE (UNII: 4CG9F9W01Q)
CETYL DIMETHICONE 45 (UNII: IK315POC44)
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
WHITE WAX (UNII: 7G1J5DA97F)
CHLORPHENESIN (UNII: I670DAL4SZ)
HEXAMETHYLDISILOXANE (UNII: D7M4659BPU)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
WATER (UNII: 059QF0KO0R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-151-09	28.4 g in 1 JAR; Type 0: Not a Combination Product	01/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	M020	01/07/2020

Labeler - H.E.B. (007924756)