SPF 50 BABY SUNSCREEN EQUATE- avobenzone, homosalate, octocrylene lotion

SPF 50 Baby Sunscreen by

Drug Labeling and Warnings

SPF 50 Baby Sunscreen by is a Otc medication manufactured, distributed, or labeled by Walmart Inc, Derma Care Research Labs, LLC, Derma Care Research Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Avobenzone 3%, Homosalate 10%, Octocrylene 6%

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 eyes with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

PREGNANCY OR BREAST FEEDING

Ask a health professional before use.

Keep Out of Reach of Children.

If product is 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

Sun protection measures: spending time n the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measure including:

• limit time in the sun, especially from 10 am to 2 pm
• wear long-sleeved shirts, pants, hats, and sunglasses.
• Children under 6 months: ask a doctor.

Inactive Ingredients

Aluminum Starch Octenylsuccinate, Butyloctyl Salicylate, Carbomer, Dimethicone, Disodium EDTA, Ethylhexylglycerin, Phenoxyethanol, Polyglceryl-3 Distearate, Sorbitan Isostearate, Sorbitol, Stearic Acid, Triethanolamine, VP/Eicosene Copolymer, Water.

Label

INGREDIENTS AND APPEARANCE

SPF 50 BABY SUNSCREEN  EQUATE
avobenzone, homosalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-360
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)
STEARIC ACID (UNII: 4ELV7Z65AP)
POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
EDETATE DISODIUM (UNII: 7FLD91C86K)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
DIMETHICONE 20 (UNII: H8YMB5QY0D)
CARBOMER 940 (UNII: 4Q93RCW27E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-360-08	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/22/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/22/2020

Labeler - Walmart Inc (051957769)

Registrant - Derma Care Research Labs, LLC (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs		116817470	manufacture(79903-360)