Label: MENTHOLATUM NATURAL ICE CHERRY- dimethicone, octinoxate, octisalate stick
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NDC Code(s):
10742-1048-1,
10742-1048-2,
10742-1048-3,
10742-1048-4, view more10742-1048-8, 10742-1048-9
- Packager: The Mentholatum Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated February 7, 2023
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- Active ingredients
- Purpose
- Uses
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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 prevent sunburn, not skin cancer or early skin aging.
For external use only
- Directions
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
MENTHOLATUM NATURAL ICE CHERRY
dimethicone, octinoxate, octisalate stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-1048 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 10 mg in 1 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) CERESIN (UNII: Q1LS2UJO3A) PETROLATUM (UNII: 4T6H12BN9U) LANOLIN (UNII: 7EV65EAW6H) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) LEVOMENTHOL (UNII: BZ1R15MTK7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-1048-1 1 in 1 BLISTER PACK 08/19/1999 04/01/2019 1 4.5 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:10742-1048-9 4.5 g in 1 TUBE; Type 0: Not a Combination Product 08/19/1999 04/01/2019 3 NDC:10742-1048-2 1 in 1 BLISTER PACK 04/02/2019 3 4.2 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:10742-1048-8 4.2 g in 1 TUBE; Type 0: Not a Combination Product 04/02/2019 5 NDC:10742-1048-3 1 in 1 BLISTER PACK 08/19/1999 5 4.5 g in 1 TUBE; Type 0: Not a Combination Product 6 NDC:10742-1048-4 4.5 g in 1 TUBE; Type 0: Not a Combination Product 08/19/1999 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 08/19/1999 Labeler - The Mentholatum Company (002105757) Registrant - The Mentholatum Company (002105757) Establishment Name Address ID/FEI Business Operations The Mentholatum Company 002105757 manufacture(10742-1048)