AVEENO SKIN RELIEF GENTLE SCENT NOURISHING COCONUT- dimethicone lotion

Aveeno Skin Relief Gentle Scent by

Drug Labeling and Warnings

Aveeno Skin Relief Gentle Scent 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 (1.3%)

Purpose

Skin Protectant

Use

• 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, Chlorphenesin, Steareth-2, Avena Sativa (Oat) Kernel Oil, Cocos Nucifera (Coconut) Oil, Dipropylene Glycol, Ethylene Brassylate, Gamma-Nonalactone, Tetramethyl Acetyloctahydronaphthalenes, Cetyl Hydroxyethylcellulose, Sodium Chloride, Avena Sativa (Oat) Kernel Extract

Questions?

Call 866-428-3366 or www.aveeno.com

SPL UNCLASSIFIED SECTION

Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558-9418

PRINCIPAL DISPLAY PANEL - 354 mL Bottle Label

new
gentle scent
Aveeno®
ACTIVE NATURALS®

skin relief
gentle scent lotion

nourishing coconut
dimethicone skin protectant

as gentle as fragrance free™
relieves itchy, extra-dry skin

CLINICALLY TESTED
THERAPEUTIC
TRIPLE OAT FORMULA

DERMATOLOGIST
RECOMMENDED
12 FL. OZ. (354 mL)

INGREDIENTS AND APPEARANCE

AVEENO SKIN RELIEF GENTLE SCENT   NOURISHING COCONUT
dimethicone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Dimethicone (UNII: 92RU3N3Y1O) (Dimethicone - UNII:92RU3N3Y1O)	Dimethicone	13 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)
Chlorphenesin (UNII: I670DAL4SZ)
Steareth-2 (UNII: V56DFE46J5)
Oat Kernel Oil (UNII: 3UVP41R77R)
Coconut Oil (UNII: Q9L0O73W7L)
Dipropylene Glycol (UNII: E107L85C40)
Ethylene Brassylate (UNII: 9A87HC7ROD)
.Gamma.-Nonalactone (UNII: I1XGH66S8P)
Tetramethyl Acetyloctahydronaphthalenes (UNII: 2JU6ZH6GRE)
Sodium Chloride (UNII: 451W47IQ8X)
Oat (UNII: Z6J799EAJK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0002-1	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2015	07/23/2020
2	NDC: 69968-0002-2	354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2015	11/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part347	08/01/2015	11/26/2020

Labeler - Johnson & Johnson Consumer Inc. (002347102)