CVS HEALTH BABY SPF 50 SUN- octinoxate, octisalate, zinc oxide lotion 
CVS Pharmacy

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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CVS Health Baby SPF 50 Sun Lotion

Active ingredients

Octinoxate 7.5%, Octisalate 5.0%, Zinc Oxide 14.5%

Purpose

Sunscreen

Uses

Warnings

​For external use only

​Do not use

​When using this product​

keep out of eyes. Rinse with water to remove.

Stop use and ask doctor if

rash occurs.

​Keep out of reach of children. ​

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

Directions

Inactive ingredients

water, propylene glycol, c12-15 alkyl benzoate, neopentyl glycol diheptanoate, cyclopentasiloxane, cetyl PEG/PPG-10/1 dimethicone, PEG-12 dimethicone crosspolymer, triethoxycaprylylsilane, aloe barbadensis leaf extract, ethylhexyl palmitate, diazolidinyl urea, methylparaben, propylparaben, sodium chloride

Other information

• protect the product in this container from excessive heat and direct sun
• may stain or damage some fabrics, materials or surfaces

Label

CVS35232EF

CVS47134A

CVS HEALTH  BABY SPF 50 SUN
octinoxate, octisalate, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-138
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE145 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-138-11237 mL in 1 BOTTLE; Type 0: Not a Combination Product02/10/2017
2NDC:69842-138-22177 mL in 1 BOTTLE; Type 0: Not a Combination Product03/09/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35203/09/2016
Labeler - CVS Pharmacy (062312574)

Revised: 12/2022
Document Id: f05dffc1-20bf-ddd6-e053-2995a90aab21
Set id: 483298ff-b94b-1fea-e054-00144ff8d46c
Version: 4
Effective Time: 20221221
 
CVS Pharmacy