Label: BLUESTOP MAX- external analgesic gel
- NDC Code(s): 82714-001-01
- Packager: Clavel Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 15, 2024
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Inactive Ingredients
Aloe Vera Leaf, Alpha-Tocopherol Acetate, Ammonium Acryloyldimethyltaurate, Dimethylacrylamide, Lauryl Methacrylate and Laureth-4 Methacrylate Copolymer, Trimethylolpropane Triacrylate Crosslinked (45000 Mpa.S), Cetyl Alcohol, Coconut Oil, Dimethyl Sulfone, Ethylhexylglycerin,Ethylhexyl Palmitate, Fragrance, Garcinia Indica Seed Butter, Glucosamine Sulfate, Glycerin, Melaleuca Alternifolia Leaf, Phenoxyethanol, Sodium Acrylate/Sodium Acryloyldimethyltaurate Copolymer (4000000 MW), Vitamin A Palmitate, Water, Witch Hazel
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INGREDIENTS AND APPEARANCE
BLUESTOP MAX
external analgesic gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82714-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 10 mg in 1 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 40 mg in 1 g Inactive Ingredients Ingredient Name Strength WITCH HAZEL (UNII: 101I4J0U34) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) GARCINIA INDICA SEED BUTTER (UNII: US2H3D7800) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) CETYL ALCOHOL (UNII: 936JST6JCN) COCONUT OIL (UNII: Q9L0O73W7L) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYL PALMITATE (UNII: 2865993309) AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82714-001-01 1 in 1 CARTON 01/10/2023 1 85 g in 1 APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 01/10/2023 Labeler - Clavel Corporation (927855643) Establishment Name Address ID/FEI Business Operations TAKA USA Inc, dba Cosmetic Innovations 802860515 manufacture(82714-001)