CHAPSTICK MOISTURIZER- octinoxate, oxybenzone, petrolatum gel 
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ChapStick Moisturizer
(octinoxate, oxybenzone, white petrolatum)

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

ChapStick Moisturizer Packaging
CHAPSTICK MOISTURIZER 
octinoxate, oxybenzone, petrolatum gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0573-1926
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
octinoxate (UNII: 4Y5P7MUD51) (octinoxate - UNII:4Y5P7MUD51) octinoxate75 mg  in 1 g
oxybenzone (UNII: 95OOS7VE0Y) (oxybenzone - UNII:95OOS7VE0Y) oxybenzone35 mg  in 1 g
petrolatum (UNII: 4T6H12BN9U) (petrolatum - UNII:4T6H12BN9U) petrolatum330 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Product Characteristics
ColorYELLOW (opaque light yellow) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0573-1926-121 in 1 BLISTER PACK01/01/200406/28/2018
110 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34701/01/200406/28/2018
Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)

Revised: 5/2021
Document Id: 19839014-8581-4d00-a958-287f7f7f44cf
Set id: 109022e9-7bd1-e5c2-1fc7-d9c978a6c603
Version: 2
Effective Time: 20210504
 
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC