CHAPSTICK MOISTURIZER- octinoxate, oxybenzone, petrolatum gel

CHAPSTICK MOISTURIZER by

Drug Labeling and Warnings

CHAPSTICK MOISTURIZER by is a Otc medication manufactured, distributed, or labeled by Wyeth Consumer Healthcare. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

ACTIVE INGREDIENTS

Octinoxate 7.5%

Oxybenzone 3.5%

White petrolatum 33.0%

PURPOSES

Sunscreen

Sunscreen

Skin Protectant

USES

• helps prevent sunburn
• higher SPF gives more sunburn protection
• helps prevent and temporarily protects chafed, chapped, cracked, or windburned lips

WARNINGS

For external use only

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

• rash or irritation develops and lasts
• condition worsens or does not improve within 7 days

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

• apply liberally before sun exposure and as needed
• children under 6 months of age: ask a doctor

OTHER INFORMATION

store at 20-25ºC (68-77ºF)

INACTIVE INGREDIENTS

aloe barbadensis leaf extract, fragrance, isocetyl stearate, lanolin, methylparaben, microcrystalline wax, mineral oil, propylparaben, tocopheryl linoleate/oleate, vitamin E acetate

PRODUCT PACKAGING

The product packaging shown below represents a sample of that currently in use. Additional packaging may also be available.

ChapStick Moisturizer

Skin Protectant / Sunscreen SPF 15

ANGLED TIP

GLIDES ON EASILY

Softens & Protects Lips Every Day with an Ultra-Hydrating Formula

NET WT .35 OZ (10g)

Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

Wyeth Consumer Healthcare, Madison, NJ 07940

Made in USA ©2006 Wyeth

www.chapstick.com

INGREDIENTS AND APPEARANCE

CHAPSTICK MOISTURIZER 
octinoxate, oxybenzone, petrolatum gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0573-1926
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
octinoxate (UNII: 4Y5P7MUD51) (octinoxate - UNII:4Y5P7MUD51)	octinoxate	75 mg  in 1 g
oxybenzone (UNII: 95OOS7VE0Y) (oxybenzone - UNII:95OOS7VE0Y)	oxybenzone	35 mg  in 1 g
petrolatum (UNII: 4T6H12BN9U) (petrolatum - UNII:4T6H12BN9U)	petrolatum	330 mg  in 1 g

Product Characteristics
Color	YELLOW (opaque light yellow)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0573-1926-12	1 in 1 BLISTER PACK
1		10 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	01/01/2004

Labeler - Wyeth Consumer Healthcare (828831730)