AVEENO BABY CONTINUOUS PROTECTION SENSITIVE SKIN SUNSCREEN BROAD SPECTRUM SPF50- zinc oxide lotion 
Johnson & Johnson Consumer Inc.

----------

Aveeno Baby ® CONTINUOUS PROTECTION ® sensitive skin sunscreen

BROAD SPECTRUM SPF 50

Drug Facts

Active Ingredient

Zinc Oxide 21.6%

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

Other Information

Inactive Ingredients

Water, C 12-15 Alkyl Benzoate, Styrene/Acrylates Copolymer, Octyldodecyl Citrate Crosspolymer, Phenyl Trimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Dimethicone, Polyhydroxystearic Acid, Glycerin, Ethyl Methicone, Silica, Cetyl Dimethicone, Triethoxycaprylylsilane, Phenoxyethanol, Glyceryl Behenate, Sodium Chloride, Acrylates/Dimethicone Copolymer, Chlorphenesin, Phenethyl Alcohol, Avena Sativa (Oat) Kernel Flour, Caprylyl Glycol, Cetyl Dimethicone/Bis-Vinyldimethicone Crosspolymer, Chrysanthemum Parthenium (Feverfew)Flower/Leaf/Stem Juice

Questions

866-428-3366; Outside US , dial collect 215-273-8755 www.aveeno.com

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 207 mL Tube Label

PEDIATRICIAN
RECOMMENDED BRAND
Aveeno
Baby ®
CONTINUOUS
PROTECTION ®
sensitive skin
zinc oxide
sunscreen
BROAD SPECTRUM SPF 50
naturally-sourced 100%
mineral active ingredient

sweat + water resistant
(80 min)
SPF
50
7.0 fl oz (mL)

Principal Display Panel - 207 mL Tube Label
AVEENO BABY CONTINUOUS PROTECTION SENSITIVE SKIN  SUNSCREEN BROAD SPECTRUM SPF50
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0304
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE216 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
GLYCERIN (UNII: PDC6A3C0OX)  
ETHYL METHICONE (8 MPA.S) (UNII: 3YWG8XYT8H)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
OATMEAL (UNII: 8PI54V663Y)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
FEVERFEW (UNII: Z64FK7P217)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: X323T6QO4M)  
CETYL DIMETHICONE/BIS-VINYLDIMETHICONE CROSSPOLYMER (UNII: AE7QA6TW0Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0304-114 mL in 1 TUBE; Type 0: Not a Combination Product10/01/201602/28/2024
2NDC:69968-0304-388 mL in 1 TUBE; Type 0: Not a Combination Product10/01/2016
3NDC:69968-0304-62 in 1 TRAY11/20/201901/23/2025
3NDC:69968-0304-388 mL in 1 TUBE; Type 0: Not a Combination Product
4NDC:69968-0304-7207 mL in 1 TUBE; Type 0: Not a Combination Product12/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/01/2016
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 4/2024
Document Id: 16611879-e520-a822-e063-6294a90af9e5
Set id: bbd6710f-a665-437e-b86b-437f732984d1
Version: 8
Effective Time: 20240418
 
Johnson & Johnson Consumer Inc.