AVEENO ACTIVE NATURALS DAILY MOISTURIZING- dimethicone lotion

Aveeno Active Naturals Daily Moisturizing by

Drug Labeling and Warnings

Aveeno Active Naturals Daily Moisturizing 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
• Helps prevent and protect from the drying effects of wind and cold weather

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

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?

Call toll free 866-4AVEENO 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®
ACTIVE NATURALS®

daily moisturizing
lotion
dimethicone skin protectant

clinically proven to
relieve dry skin

moisturizes for 24 hours
fragrance free

DERMATOLOGIST
RECOMMENDED
ACTIVE NATURALS®
SOOTHING
OATMEAL

18 fl. oz. (532 mL)

INGREDIENTS AND APPEARANCE

AVEENO ACTIVE NATURALS DAILY MOISTURIZING 
dimethicone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0003
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)
Sodium Chloride (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0003-8	532 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/01/2004	10/01/2020
2	NDC: 69968-0003-7	354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/01/2004	10/22/2020
3	NDC: 69968-0003-4	227 mL in 1 TUBE; Type 0: Not a Combination Product	02/01/2004	12/15/2020
4	NDC: 69968-0003-5	141 mL in 1 TUBE; Type 0: Not a Combination Product	06/01/2013	04/09/2022
5	NDC: 69968-0003-2	71 mL in 1 TUBE; Type 0: Not a Combination Product	06/01/2013	11/19/2020
6	NDC: 69968-0003-1	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2004	11/05/2020
7	NDC: 69968-0003-3	24 in 1 CARTON	02/01/2004	04/09/2022
7	NDC: 69968-0003-1	29 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part347	02/01/2004	04/09/2022

Labeler - Johnson & Johnson Consumer Inc. (002347102)