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]

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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 - 532 mL Bottle Label

Aveeno
Baby®

PEDIATRICIAN
Aveeno®
RECOMMENDED®

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

Dimethicone Skin Protectant
with Natural Colloidal Oatmeal

Protects Delicate Skin
Moisturizes for 24 Hours

18 FL. OZ. (532 mL)

INGREDIENTS AND APPEARANCE

AVEENO BABY DAILY MOISTURE 
dimethicone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0441
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)
Oat (UNII: Z6J799EAJK)
Benzyl Alcohol (UNII: LKG8494WBH)
Sodium Chloride (UNII: 451W47IQ8X)
Allantoin (UNII: 344S277G0Z)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0441-8	227 mL in 1 TUBE; Type 0: Not a Combination Product	08/01/2001
2	NDC: 69968-0441-1	532 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2001
3	NDC: 69968-0441-2	354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2001
4	NDC: 69968-0441-3	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2001

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

Labeler - Johnson & Johnson Consumer Inc. (002347102)