Label: SOFTLIPS OASIS PINEAPPLE COCONUT- dimethicone, oxybenzone, octinoxate stick
- NDC Code(s): 10742-8745-1, 10742-8745-2
- Packager: The Mentholatum Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
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- Active ingredient
- Purpose
- Uses
- Warnings
- Keep Out of Reach of Children
- Directions
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Inactive ingredients
ozokerite, petrolatum, mineral oil, octyldodecanol, ethylhexyl palmitate, polyglyceryl-6 octastearate, cetearyl alcohol, flavor, polyglyceryl-6 polyricinoleate, sea water, VP/eicosene copolymer, ammonium glycyrrhizate, ananas sativus (pineapple) fruit extract, butylene glycol, carthamus tinctorius (safflower) seed oil, cetearyl glucoside, cocos nucifera (coconut) extract, ethylhexylglycerin, hyaluronic acid, limnanthes alba (meadowfoam) seed oil, menthol, nannochloropsis oculata extract, pentylene glycol, phenoxyethanol, phytosteryl/octyldodecyl lauroyl glutamate, porphyra umbilicalis extract, silanetriol, silybum marianum seed oil, tetrahexyldecyl ascorbate [vitamin C], tocopheryl acetate [vitamin E]
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INGREDIENTS AND APPEARANCE
SOFTLIPS OASIS PINEAPPLE COCONUT
dimethicone, oxybenzone, octinoxate stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-8745 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 20 mg in 1 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 40 mg in 1 g Inactive Ingredients Ingredient Name Strength CERESIN (UNII: Q1LS2UJO3A) PETROLATUM (UNII: 4T6H12BN9U) MINERAL OIL (UNII: T5L8T28FGP) OCTYLDODECANOL (UNII: 461N1O614Y) ETHYLHEXYL PALMITATE (UNII: 2865993309) POLYGLYCERYL-6 DISTEARATE (UNII: Z35I17EQOP) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W) SODIUM CHLORIDE (UNII: 451W47IQ8X) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C) PINEAPPLE (UNII: 2A88ZO081O) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SAFFLOWER OIL (UNII: 65UEH262IS) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) COCONUT (UNII: 3RT3536DHY) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HYALURONIC ACID (UNII: S270N0TRQY) MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y) RACEMENTHOL (UNII: YS08XHA860) PHYMATOLITHON CALCAREUM (UNII: 6J1M3WA0ZK) PENTYLENE GLYCOL (UNII: 50C1307PZG) PHENOXYETHANOL (UNII: HIE492ZZ3T) PHYTOSTERYL/OCTYLDODECYL LAUROYL GLUTAMATE (UNII: 65954KGO9Q) PORPHYRA UMBILICALIS (UNII: 14AN0J70WO) SILANETRIOL (UNII: E52D0J3TS5) SILYBUM MARIANUM SEED OIL (UNII: NYY23HEN06) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-8745-1 1 in 1 BLISTER PACK 05/01/2019 1 4.5 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:10742-8745-2 4.5 g in 1 TUBE; Type 0: Not a Combination Product 07/15/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/01/2019 Labeler - The Mentholatum Company (002105757) Registrant - The Mentholatum Company (002105757) Establishment Name Address ID/FEI Business Operations The Mentholatum Company 002105757 manufacture(10742-8745)