AVEENO DAILY MOISTURIZING- dimethicone lotion

Aveeno DAILY MOISTURIZING by

Drug Labeling and Warnings

Aveeno 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 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 immediately.

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?

866-428-3366; outside US, dial collect 215-273-8755 www.aveeno.com

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 591 mL Bottle Label

NEW LOOK
SAME GREAT FORMULA

Aveeno®
DAILY
MOISTURIZING
Lotion
Dimethicone skin protectant
Nourishes
Dry Skin
Clinically proven
healthier-looking
skin in 1 day

fragrance
free

with
SOOTHING OAT
& RICH EMOLLIENTS
20 fl oz (591 mL)

INGREDIENTS AND APPEARANCE

AVEENO DAILY MOISTURIZING 
dimethicone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0454
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0454-3	532 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/01/2004
2	NDC: 69968-0454-1	354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/01/2004
3	NDC: 69968-0454-8	227 mL in 1 TUBE; Type 0: Not a Combination Product	02/01/2004
4	NDC: 69968-0454-5	141 mL in 1 TUBE; Type 0: Not a Combination Product	06/01/2013
5	NDC: 69968-0454-4	71 mL in 1 TUBE; Type 0: Not a Combination Product	06/01/2013
6	NDC: 69968-0454-6	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2004
7	NDC: 69968-0454-2	591 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/01/2016

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

Labeler - Johnson & Johnson Consumer Inc. (002347102)