Label: CHAPSTICK MOISTURIZER VARIETY PACK- avobenzone, homosalate, octisalate, octocrylene, white petrolatum kit
- NDC Code(s): 0573-0158-01, 0573-1057-01, 0573-1956-01, 0573-1959-01
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 12, 2024
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- Official Label (Printer Friendly)
- Active ingredients (Original)
- Active ingredients (Cool Mint)
- Active ingredients (Black Cherry)
- Purposes
- Uses
- Warnings
- Directions
- Other information
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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)
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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
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INGREDIENTS AND APPEARANCE
CHAPSTICK MOISTURIZER VARIETY PACK
avobenzone, homosalate, octisalate, octocrylene, white petrolatum kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-1959 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0573-1959-01 1 in 1 KIT; Type 0: Not a Combination Product 04/01/2022 Quantity of Parts Part # Package Quantity Total Product Quantity 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 stickProduct Information Item Code (Source) NDC:0573-0158 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 Inactive Ingredients Ingredient Name Strength 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0573-0158-01 4 g in 1 CYLINDER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 04/01/2022 Part 2 of 3 CHAPSTICK COOL MINT
avobenzone, homosalate, octisalate, octocrylene, white petrolatum stickProduct Information Item Code (Source) NDC:0573-1057 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 Inactive Ingredients Ingredient Name Strength 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0573-1057-01 4 g in 1 CYLINDER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 04/01/2022 Part 3 of 3 CHAPSTICK BLACK CHERRY
avobenzone, homosalate, octisalate, octocrylene, white petrolatum stickProduct Information Item Code (Source) NDC:0573-1956 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 Inactive Ingredients Ingredient Name Strength 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0573-1956-01 4 g in 1 CYLINDER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 04/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 04/01/2022 Labeler - Haleon US Holdings LLC (079944263)
