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NDC 00573-1959-01 Chapstick Moisturizer Variety Pack Details

Chapstick Moisturizer Variety Pack

Chapstick Moisturizer Variety Pack is a KIT in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is .

Product Information

NDC	00573-1959
Product ID	0573-1959_bfb9a2d5-1ad2-45b8-a215-9d1370af5337
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Chapstick Moisturizer Variety Pack
Proprietary Name Suffix	n/a
Non-Proprietary Name	avobenzone, homosalate, octisalate, octocrylene, white petrolatum
Product Type	HUMAN OTC DRUG
Dosage Form	KIT
Route	n/a
Active Ingredient Strength	n/a
Active Ingredient Units	n/a
Substance Name	n/a
Labeler Name	GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part347
Listing Certified Through	2024-12-31

Package

Package Images

NDC 00573-1959-01 (00573195901)

Pricing Information	N/A
NDC Package Code	0573-1959-01
Billing NDC	00573195901
Package	1 KIT in 1 KIT (0573-1959-01) * 4 g in 1 CYLINDER (0573-1057-01) * 4 g in 1 CYLINDER (0573-1956-01) * 4 g in 1 CYLINDER (0573-0158-01)
Marketing Start Date	2022-04-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL bfb9a2d5-1ad2-45b8-a215-9d1370af5337 Details

Active ingredients (Original)

Avobenzone 3.0%

Homosalate 4.0%

Octisalate 4.5%

Octocrylene 2.6%

White Petrolatum 38.4%

Active ingredients (Cool Mint)

Avobenzone 3.0%

Homosalate 4.0%

Octisalate 4.5%

Octocrylene 2.6%

White Petrolatum 36.9%

Active ingredients (Black Cherry)

Avobenzone 3.0%

Homosalate 4.0%

Octisalate 4.5%

Octocrylene 2.6%

White Petrolatum 36.8%

Purposes

Sunscreens

Skin protectant

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

Warnings

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

Do not use on damaged or broken skin

Stop use and ask a doctor if rash occurs

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

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

Directions

•: 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

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

Inactive ingredients (Original)

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)

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)

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?

1-800-245-1040

Additional information

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.

PRINCIPAL DISPLAY PANEL

NEW

Formula

BRAND LIP CARE

ChapStick®

SKIN PROTECTANT | SUNSCREEN

SPF 12

MOISTURIZER

2 in 1 Lipcare Variety Pack

8 HOUR MOISTURE

SPF 12

3 STICKS

NET WT 0.15 OZ

(4 g) EACH

000073773

INGREDIENTS AND APPEARANCE

CHAPSTICK MOISTURIZER VARIETY PACK

avobenzone, homosalate, octisalate, octocrylene, white petrolatum kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0573-1959

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0573-1959-01	1 in 1 KIT; Type 0: Not a Combination Product	04/01/2022

Part #	Package Quantity	Total Product Quantity
Quantity of Parts
Part 1	1 CYLINDER	4 g
Part 2	1 CYLINDER	4 g
Part 3	1 CYLINDER	4 g

Part 1 of 3
CHAPSTICK ORIGINAL avobenzone, homosalate, octisalate, octocrylene, white petrolatum stick

Product Information
Item Code (Source)	NDC:0573-0158
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	40 mg in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	45 mg in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	26 mg in 1 g
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	384 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
ANISYL ALCOHOL (UNII: 7N6XGV3U49)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BENZYL BENZOATE (UNII: N863NB338G)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CETYL ALCOHOL (UNII: 936JST6JCN)
CARNAUBA WAX (UNII: R12CBM0EIZ)
ISOCETYL STEARATE (UNII: 3RJ7186O9W)
LANOLIN (UNII: 7EV65EAW6H)
MINERAL OIL (UNII: T5L8T28FGP)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
PARAFFIN (UNII: I9O0E3H2ZE)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
TOCOPHEROL (UNII: R0ZB2556P8)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WHITE WAX (UNII: 7G1J5DA97F)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0573-0158-01	4 g in 1 CYLINDER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	04/01/2022

Part 2 of 3
CHAPSTICK COOL MINT avobenzone, homosalate, octisalate, octocrylene, white petrolatum stick

Product Information
Item Code (Source)	NDC:0573-1057
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	40 mg in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	45 mg in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	26 mg in 1 g
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	369 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CETYL ALCOHOL (UNII: 936JST6JCN)
CARNAUBA WAX (UNII: R12CBM0EIZ)
ISOCETYL STEARATE (UNII: 3RJ7186O9W)
LANOLIN (UNII: 7EV65EAW6H)
MINERAL OIL (UNII: T5L8T28FGP)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
PARAFFIN (UNII: I9O0E3H2ZE)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
TOCOPHEROL (UNII: R0ZB2556P8)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WHITE WAX (UNII: 7G1J5DA97F)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0573-1057-01	4 g in 1 CYLINDER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	04/01/2022

Part 3 of 3
CHAPSTICK BLACK CHERRY avobenzone, homosalate, octisalate, octocrylene, white petrolatum stick

Product Information
Item Code (Source)	NDC:0573-1956
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	40 mg in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	45 mg in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	26 mg in 1 g
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	384 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
FD&C BLUE NO. 1--ALUMINUM LAKE (UNII: J9EQA3S2JM)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETYL ALCOHOL (UNII: 936JST6JCN)
CARNAUBA WAX (UNII: R12CBM0EIZ)
ISOCETYL STEARATE (UNII: 3RJ7186O9W)
ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
LANOLIN (UNII: 7EV65EAW6H)
MINERAL OIL (UNII: T5L8T28FGP)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
PARAFFIN (UNII: I9O0E3H2ZE)
D&C RED NO. 6 (UNII: 481744AI4O)
D&C RED NO. 7 (UNII: ECW0LZ41X8)
ALUMINUM OXIDE (UNII: LMI26O6933)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
SACCHARIN (UNII: FST467XS7D)
SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)
TOCOPHEROL (UNII: R0ZB2556P8)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
.ALPHA.-TOCOPHEROL LINOLEATE, D- (UNII: G0N132Q0ED)
WHITE WAX (UNII: 7G1J5DA97F)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0573-1956-01	4 g in 1 CYLINDER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	04/01/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	04/01/2022

Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)

Revised: 2/2022

Document Id: bfb9a2d5-1ad2-45b8-a215-9d1370af5337

Set id: bfb9a2d5-1ad2-45b8-a215-9d1370af5337

Version: 1

Effective Time: 20220228

Search by Drug Name or NDC

NDC 00573-1959-01 Chapstick Moisturizer Variety Pack Details

Chapstick Moisturizer Variety Pack

Product Information

Package

Package Images

NDC 00573-1959-01 (00573195901)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL bfb9a2d5-1ad2-45b8-a215-9d1370af5337 Details

Active ingredients (Original)

Active ingredients (Cool Mint)

Active ingredients (Black Cherry)

Purposes

Uses

Warnings

Directions

Other information

Inactive ingredients (Original)

Inactive ingredients (Cool Mint)

Inactive ingredients (Black Cherry)

Questions?

Additional information

PRINCIPAL DISPLAY PANEL

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