AVEENO BABY DAILY MOISTURE- dimethicone lotion 
Johnson & Johnson Consumer Inc.

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Aveeno® baby daily moisture lotion

Drug Facts

Active ingredient

Dimethicone 1.2%

Purpose

Skin Protectant

Uses

Warnings

For external use only

When using this product

  • Do not get into eyes

Stop use and ask a doctor if

  • Condition worsens
  • Symptoms last more than 7 days or clear up and occur again within a few days

Do not use on

  • Deep or puncture wounds
  • Animal bites
  • Serious burns

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, Glycerin, Distearyldimonium Chloride, Petrolatum, Isopropyl Palmitate, Cetyl Alcohol, Avena Sativa (Oat) Kernel Flour, Benzyl Alcohol, Sodium Chloride, Allantoin

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 - 227 g Tube Label

RECOMMENDED BY
PEDIATRICIANS
& DERMATOLOGISTS

Aveeno®
baby

NEW
LOOK
Same Great
Formula

daily moisture
lotion

natural oatmeal
dimethicone skin protectant

protects &
moisturizes
baby's sensitive
skin for 24hrs

fragrance-free
hypoallergic

NET WT. 8 OZ (227 g)

Principal Display Panel - 227 g Tube Label
AVEENO BABY DAILY MOISTURE 
dimethicone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0679
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE12 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)  
PETROLATUM (UNII: 4T6H12BN9U)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
OAT (UNII: Z6J799EAJK)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
ALLANTOIN (UNII: 344S277G0Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0679-8227 g in 1 TUBE; Type 0: Not a Combination Product08/01/2001
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01608/01/2001
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2024
Document Id: 1012a0a9-8b40-8ed1-e063-6394a90a1003
Set id: 3879110f-ba83-446b-b580-f8eaa859789d
Version: 3
Effective Time: 20240129
 
Johnson & Johnson Consumer Inc.