AVEENO BABY DAILY MOISTURE- dimethicone lotion

Aveeno Baby Daily Moisture by

Drug Labeling and Warnings

Aveeno Baby Daily Moisture by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Dimethicone 1.2%

Purpose

Skin Protectant

Uses

• Helps prevent and temporarily protects chafed, chapped or cracked skin

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

• Apply as needed.

Other information

• To open, twist off cap and remove quality seal. Do not use if quality seal is broken.
• Store at room temperature.

Inactive ingredients

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

Questions?

Call toll-free 866-4 AVEENO or 215-273-8755 (collect) www.aveeno.com

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Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 227 g Tube Label

Aveeno
Baby®

PEDIATRICIAN
Aveeno®
RECOMMENDED®

FRAGRANCE-REE. PARABEN-FREE
PHTHALATE-FREE
Daily Moisture Lotion

Dimethicone Skin Protectant
with Natural Colloidal Oatmeal

Protects Delicate Skin
Moisturizes for 24 Hours

NET WT. 8 OZ. (227 g)

INGREDIENTS AND APPEARANCE

AVEENO BABY DAILY MOISTURE 
dimethicone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0039
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Dimethicone (UNII: 92RU3N3Y1O) (Dimethicone - UNII:92RU3N3Y1O)	Dimethicone	12 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Distearyldimonium Chloride (UNII: OM9573ZX3X)
Petrolatum (UNII: 4T6H12BN9U)
Isopropyl Palmitate (UNII: 8CRQ2TH63M)
Cetyl Alcohol (UNII: 936JST6JCN)
Oatmeal (UNII: 8PI54V663Y)
Benzyl Alcohol (UNII: LKG8494WBH)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Allantoin (UNII: 344S277G0Z)
Sodium Chloride (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0039-8	227 mL in 1 TUBE; Type 0: Not a Combination Product	08/01/2001	01/04/2020
2	NDC: 69968-0039-9	354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2001	01/16/2021
3	NDC: 69968-0039-7	532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2001	01/14/2021
4	NDC: 69968-0039-2	29.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2001	01/21/2021
5	NDC: 69968-0039-1	29.5 mL in 1 TUBE; Type 0: Not a Combination Product	08/01/2001	04/09/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part347	08/01/2001	04/09/2022

Labeler - Johnson & Johnson Consumer Inc. (002347102)