FDA.reportPublic FDA data

Chapstick Moisturizer Variety Pack

Manufacturer
Haleon US Holdings LLC
Effective date
2024-04-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:11:02

Label at a glance#

ProductChapstick Moisturizer Variety Pack
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, PETROLATUM
Label structure13 sections

Indications and uses

helps prevent sunburn helps prevent and temporarily protects chafed, chapped or cracked lips helps prevent and protect from the drying effects of wind and cold weather

Dosage and administration

apply liberally 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating children under 6 months of age: Ask a doctor

Storage and handling

store at 20-25°C (68-77°F) protect the product from excessive heat and direct sun

Label contents#

Full prescribing information#

Active ingredients (Original)

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%

Homosalate 4.0%

Octisalate 4.5%

Octocrylene 2.6%

White Petrolatum 38.4%

Active ingredients (Cool Mint)

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%

Homosalate 4.0%

Octisalate 4.5%

Octocrylene 2.6%

White Petrolatum 36.9%

Active ingredients (Black Cherry)

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%

Homosalate 4.0%

Octisalate 4.5%

Octocrylene 2.6%

White Petrolatum 36.8%

Purposes

OTC - PURPOSE SECTION

Sunscreens

Skin protectant

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • helps prevent and temporarily protects chafed, chapped or cracked lips
  • helps prevent and protect from the drying effects of wind and cold weather

Warnings

WARNINGS SECTION

Skin Cancer/ Skin Aging Alert:Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

For external use only

OTC - DO NOT USE SECTION

Do not useon damaged or broken skin

OTC - STOP USE SECTION

Stop use and ask a doctor ifrash occurs

OTC - WHEN USING SECTION

When using this productkeep out of eyes. Rinse with water to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally 15 minutes before sun exposure
  • reapply at least every 2 hours
  • use a water resistant sunscreen if swimming or sweating
  • children under 6 months of age: Ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • store at 20-25°C (68-77°F)
  • protect the product from excessive heat and direct sun

Inactive ingredients (Original)

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf extract, alpha-isomethyl ionone, anise alcohol, benzyl alcohol, benzyl benzoate, benzyl salicylate, BHT, cetyl alcohol, copernicia cerifera (carnauba) wax, fragrance, isocetyl stearate, isopropyl lanolate, lanolin, mineral oil, myristyl alcohol, paraffin, stearyl alcohol, tocopherol, tocopheryl acetate, tocopheryl linoleate/oleate, white beeswax

Inactive ingredients (Cool Mint)

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf extract, benzyl alcohol, BHT, cetyl alcohol, copernicia cerifera, (carnauba) wax, flavor, isocetyl stearate, isopropyl lanolate, lanolin, mineral oil, myristyl alcohol, paraffin, stearyl alcohol, tocopherol, tocopheryl acetate, tocopheryl linoleate/oleate, white beeswax

Inactive ingredients (Black Cherry)

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf extract, BHT, blue 1 lake, caprylic/capric triglyceride, cetyl alcohol, copernicia cerifera (carnauba) wax, isocetyl stearate, isopropyl lanolate, isopropyl titanium triisostearate, lanolin, mineral oil, myristyl alcohol, natural flavor, paraffin, red 6 lake, red 7 lake, stearyl alcohol, synthetic wax,

tocopherol, tocopheryl acetate, tocopheryl linoleate/oleate, white beeswax

Questions?

OTC - QUESTIONS SECTION

1-800-245-1040

Additional information

SPL UNCLASSIFIED SECTION

Paraben Free

Moisturizer

Variety Pack

Dist by: GSK CH, Warren, NJ 07059

For most recent product information,

visit www.chapstick.com

Trademarks owned or licensed by GSK.

©2022 GSK or licensor

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW

Formula

BRAND LIP CARE
ChapStick ®

SKIN PROTECTANT | SUNSCREEN
SPF 12

MOISTURIZER
2 in 1 Lipcare Variety Pack

8HOUR MOISTURE
SPF 12

3 STICKS

NET WT 0.15 OZ

(4 g) EACH

000073773

Chapstick Moisturizer Variety Pack 3 sticks 0.15 oz(4 g) each
Chapstick Moisturizer Variety Pack 3 sticks 0.15 oz(4 g) each

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0573-0158-01Chapstick Moisturizer Variety Pack4 g in 1 CYLINDERSTICK4 g40 mg in 1g2
0573-1057-01Chapstick Moisturizer Variety Pack4 g in 1 CYLINDERSTICK4 g369 mg in 1g2
0573-1956-01Chapstick Moisturizer Variety Pack4 g in 1 CYLINDERSTICK4 g26 mg in 1g2
0573-1959-01Chapstick Moisturizer Variety Pack1 in 1 KITKIT12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0573-0158CHAPSTICK MOISTURIZER VARIETY PACK (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM) KIT [HALEON US HOLDINGS LLC]2Unmatched20240415_bfb9a2d5-1ad2-45b8-a215-9d1370af5337.zip
0573-1057CHAPSTICK MOISTURIZER VARIETY PACK (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM) KIT [HALEON US HOLDINGS LLC]2Unmatched20240415_bfb9a2d5-1ad2-45b8-a215-9d1370af5337.zip
0573-1956CHAPSTICK MOISTURIZER VARIETY PACK (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM) KIT [HALEON US HOLDINGS LLC]2Unmatched20240415_bfb9a2d5-1ad2-45b8-a215-9d1370af5337.zip
0573-1959CHAPSTICK MOISTURIZER VARIETY PACK (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM) KIT [HALEON US HOLDINGS LLC]2Current NDC, Legacy NDC, 4 package rows20240415_bfb9a2d5-1ad2-45b8-a215-9d1370af5337.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0573-19590573-1959-01
0573-01580573-0158-01
0573-10570573-1057-01
0573-19560573-1956-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 2 · 69 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
ANISYL ALCOHOL7N6XGV3U49IACT
BENZYL ALCOHOLLKG8494WBHIACT
BENZYL BENZOATEN863NB338GIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
CETYL ALCOHOL936JST6JCNIACT
CARNAUBA WAXR12CBM0EIZIACT
ISOCETYL STEARATE3RJ7186O9WIACT
LANOLIN7EV65EAW6HIACT
MINERAL OILT5L8T28FGPIACT
MYRISTYL ALCOHOLV42034O9PUIACT
PARAFFINI9O0E3H2ZEIACT
STEARYL ALCOHOL2KR89I4H1YIACT
TOCOPHEROLR0ZB2556P8IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WHITE WAX7G1J5DA97FIACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
PETROLATUM4T6H12BN9UACTIB
ALOE VERA LEAFZY81Z83H0XIACT
BENZYL ALCOHOLLKG8494WBHIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
CETYL ALCOHOL936JST6JCNIACT
CARNAUBA WAXR12CBM0EIZIACT
ISOCETYL STEARATE3RJ7186O9WIACT
LANOLIN7EV65EAW6HIACT
MINERAL OILT5L8T28FGPIACT
MYRISTYL ALCOHOLV42034O9PUIACT
PARAFFINI9O0E3H2ZEIACT
STEARYL ALCOHOL2KR89I4H1YIACT
TOCOPHEROLR0ZB2556P8IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WHITE WAX7G1J5DA97FIACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Chapstick Moisturizer Variety PackAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUMHaleon US Holdings LLCbfb9a2d5-1ad2-45b8-a215-9d1370af53372024-04-12WarningsExact identifier
ndc (package): 0573-1959-01
ndc (package): 0573-0158-01
ndc (package): 0573-1956-01
ndc (package): 0573-1057-01
ndc (product): 0573-1959
ndc11 (package): 00573195601
ndc11 (package): 00573195901
ndc11 (package): 00573015801
ndc11 (package): 00573105701
spl id: 15e6945e-8e7a-f9da-e063-6294a90ac4be
spl set id: bfb9a2d5-1ad2-45b8-a215-9d1370af5337

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.