AVEENO DAILY MOISTURIZING- dimethicone lotion 
Johnson & Johnson Consumer Inc.

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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Aveeno® daily moisturizing 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 immediately.

Directions

Apply as needed.

Other information

Store at Room Temperature

Inactive ingredients

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

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 - 591 mL Bottle Label

NEW LOOK
SAME GREAT FORMULA

Aveeno ®
DAILY
MOISTURIZING
Lotion
Dimethicone skin protectant
Nourishes
Dry Skin
Clinically proven
healthier-looking
skin in 1 day

fragrance
free

with
SOOTHING OAT
& RICH EMOLLIENTS
20 fl oz (591 mL)

Principal Display Panel - 591 mL Bottle Label
AVEENO DAILY MOISTURIZING 
dimethicone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0454
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE12 mg  in 1 mL
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0454-3532 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/01/2004
2NDC:69968-0454-1354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/01/2004
3NDC:69968-0454-8227 mL in 1 TUBE; Type 0: Not a Combination Product02/01/200407/02/2020
4NDC:69968-0454-5141 mL in 1 TUBE; Type 0: Not a Combination Product06/01/201307/02/2020
5NDC:69968-0454-471 mL in 1 TUBE; Type 0: Not a Combination Product06/01/201307/02/2020
6NDC:69968-0454-629 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/200401/26/2022
7NDC:69968-0454-2591 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/01/2016
8NDC:69968-0454-92 in 1 CARTON12/01/2016
8NDC:69968-0454-2591 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34702/01/2004
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: eeaa3f9f-cdbb-268b-e053-2a95a90a78e4
Set id: 54a13b85-32b5-439d-a27a-8fba2cf44251
Version: 13
Effective Time: 20230106
 
Johnson & Johnson Consumer Inc.