CVS HEALTH BABY SPF 50 MINERAL-BASED 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 Mineral-Based 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 swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

• protect this product from excessive heat and direct sun

• may stain or damage some fabrics, materials or surfaces

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 juice, ethylhexyl palmitate, diazolidinyl urea, methylparaben, propylparaben, sodium chloride

CVS Health Baby SPF 50 Mineral Based Lotion

CVS Health Baby SPF 50 Mineral Based Lotion

NDC 69842-178-22

6 fl oz (177 mL)

CVS59163A1

CVS Health Baby SPF 50 Mineral Based Lotion

NDC 69842-178-11

8.0 fl oz (237 mL)

CVS52269EF

CVS HEALTH  BABY SPF 50 MINERAL-BASED SUN
octinoxate, octisalate, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-178
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)  
CYCLOMETHICONE 4 (UNII: CZ227117JE)  
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:69842-178-22177 mL in 1 BOTTLE; Type 0: Not a Combination Product03/09/2018
2NDC:69842-178-11237 mL in 1 BOTTLE; Type 0: Not a Combination Product03/09/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35203/09/2018
Labeler - CVS Pharmacy (062312574)

Revised: 12/2020
Document Id: b7a5b305-3eae-077b-e053-2a95a90a30a1
Set id: 66fa70b8-ea9c-3bcd-e053-2991aa0acda2
Version: 2
Effective Time: 20201229
 
CVS Pharmacy