YOUTH TO THE PEOPLE YOUTHSCREEN SUNSCREEN BROAD SPECTRUM SPF 60- avobenzone, homosalate and octisalate cream

Youth to the People Youthscreen Sunscreen Broad Spectrum SPF 60 by

Drug Labeling and Warnings

Youth to the People Youthscreen Sunscreen Broad Spectrum SPF 60 by is a Otc medication manufactured, distributed, or labeled by L’Oreal USA Products Inc, L'OREAL USA, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Avobenzone 3%

Homosalate 15%

Octisalate 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

For sunscreen use:

• shake well before use
• apply generously 15 minutes before sun exposure
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating

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

• children under 6 months of age: Ask a doctor

Other information

protect the product in this container from excessive heat and direct sun

Inactive ingredients

water, glycerin, C15-19 alkane, propanediol, ethylhexyl methoxycrylene, butyloctyl salicylate, C12-22 alkyl acrylate/hydroxyethylacrylate copolymer, sodium stearoyl glutamate, tocopherol, cetearyl alcohol, sclerotium gum, sodium hydroxide, hydroxyacetophenone, caprylyl glycol, sodium starch octenylsuccinate, glyceryl stearate, jojoba esters, helianthus annus (sunflower) seed wax, hydroxypropyl starch phosphate, glycine soja (soybean) oil, trisodium ethylenediamine disuccinate, polyglycerin-3

Questions or comments?

PO Box 98 Westfield, NJ 07091

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INGREDIENTS AND APPEARANCE

YOUTH TO THE PEOPLE YOUTHSCREEN SUNSCREEN BROAD SPECTRUM SPF 60 
avobenzone, homosalate and octisalate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-169
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	150 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
C15-19 ALKANE (UNII: CI87N1IM01)
PROPANEDIOL (UNII: 5965N8W85T)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
TOCOPHEROL (UNII: R0ZB2556P8)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
SCLEROTIUM GUM (UNII: 2X51AD1X3T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
HELIANTHUS ANNUUS (SUNFLOWER) SEED WAX (UNII: 42DG15CHXV)
SOYBEAN OIL (UNII: 241ATL177A)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
BISABOLOL (UNII: 24WE03BX2T)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TARAXACUM OFFICINALE ROOT (UNII: 9DE5YCO0RU)
POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD)
CHAMOMILE (UNII: FGL3685T2X)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
KALE (UNII: 0Y3L4J38H1)
CITRIC ACID (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-169-01	1 in 1 CARTON	05/15/2025
1		38 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 49967-169-02	1 in 1 BLISTER PACK	05/15/2025
2		4 mL in 1 BOTTLE, DROPPER; 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	05/15/2025

Labeler - L’Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L'OREAL USA, INC.		185931458	manufacture(49967-169) , pack(49967-169)