AVEENO ACTIVE NATURALS DAILY MOISTURIZING- dimethicone cream

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]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

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

SPL UNCLASSIFIED SECTION

Distributed in the US by:
JOHNSON & JOHNSON CONSUMER PRODUCTS COMPANY
Division of Johnson & Johnson Consumer Companies, Inc.
Skillman, NJ 08558-9418

PRINCIPAL DISPLAY PANEL - 142 g Tube 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

net wt. 5 oz. (142 g)

INGREDIENTS AND APPEARANCE

AVEENO ACTIVE NATURALS DAILY MOISTURIZING 
dimethicone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58232-9907
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 g

Inactive Ingredients
Ingredient Name	Strength
OATMEAL (UNII: 8PI54V663Y)
Benzyl Alcohol (UNII: LKG8494WBH)
Cetyl Alcohol (UNII: 936JST6JCN)
Distearyldimonium Chloride (UNII: OM9573ZX3X)
Glycerin (UNII: PDC6A3C0OX)
Isopropyl Palmitate (UNII: 8CRQ2TH63M)
Petrolatum (UNII: 4T6H12BN9U)
Sodium Chloride (UNII: 451W47IQ8X)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58232-9907-8	532 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/01/2010	09/01/2019
2	NDC: 58232-9907-5	354 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/01/2010	09/01/2019
3	NDC: 58232-9907-4	226 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2010	09/01/2019
4	NDC: 58232-9907-6	142 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2010
5	NDC: 58232-9907-3	71 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2010	09/01/2019
6	NDC: 58232-9907-7	42 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2010	09/01/2019
7	NDC: 58232-9907-2	29 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2010	09/01/2019
8	NDC: 58232-9907-1	600 g in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2010
9	NDC: 58232-9907-9	2 in 1 CELLO PACK	09/01/2010
9		600 g 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	09/01/2010

Labeler - Johnson & Johnson Consumer Inc. (002347102)