WALGREENS BABY SPF50- titanium dioxide and zinc oxide lotion 
Walgreen Company

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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WAG Sun Baby Lotion SPF50 6oz

1491-23(V) Rev 01

Walgreen Baby SPF 50 Lotion

Active Ingredients

Titanium Oxide 3.30%, Zinc Oxide 4.2%

Purpose

Sunscreen

Uses

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

Inactive Ingredients

Deionized Water, Caprylic/Capric Triglycerides, Tridecyl Neopentanoate, Sorbitol, Cetyl PEG/PPG 10/1 Dimethicone, Butly Octyl Salicylate, Glycerin, Octyldodecyl Citrate Copolymer, C28-52 Olefin/Undecylenic Acid Copolymer, PEG 8, Dimethicone, Aloe Barbadensis Leaf Juice, Ethylhexyl Methoxycrylene, Tocopherol Acetate, Lauryl PEG-8 Dimethicone, Caprylyl Glycol, Sodium Chloride, Phenoxyethanol, Sodium Citrate

Other Information

Questions or comments?

www.walgreens.com or call toll free 1-800-XX-XXXX

PRINCIPAL DISPLAY PANEL

Walgreens
50

Baby

Broad spectrum SPF 50

Sunscreen UVA/UVB
HYPOALLERGENIC

OXYBENZONE FREE

TEAR
FREE
6 FL OZ (176 m
L)

Walgreens
50
Baby
Broad spectrum SPF 50
Sunscreen UVA/UVB
HYPOALLERGENIC
OXYBENZONE FREE
TEAR FREE
6 FL OZ (176 mL)

WALGREENS BABY SPF50 
titanium dioxide and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9936
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE3.1 mg  in 100 mg
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE4 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
TRIDECYL NEOPENTANOATE (UNII: 3Z8H1DA7J5)  
SORBITOL (UNII: 506T60A25R)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYOXYL 8 STEARATE (UNII: 2P9L47VI5E)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-9936-26178 mg in 1 BOTTLE; Type 0: Not a Combination Product11/15/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35211/15/2017
Labeler - Walgreen Company (008965063)
Registrant - Walgreen Company (008965063)

Revised: 8/2017
Document Id: 71378623-bd71-430b-9f1c-cf4efd8da296
Set id: f01975b7-e2c9-452f-992c-2ad1ecd1febc
Version: 1
Effective Time: 20170830
 
Walgreen Company