Label: BERKLEY JENSON ANTIBACTERIAL HAND- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 68391-151-64 - Packager: BJWC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 17, 2020
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Inactive ingredients
Water (Aqua), Cocamidopropyl Betaine, Glycerin, Decyl Glucoside, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Poloxamer 124, Polyquaternium-7, Tetrasodium EDTA, Citric Acid, Sodium Citrate, Camellia Sinensis Leaf Extract, Saccharomyces Ferment, Tocopheryl Acetate, Retinyl Palmitate, Ascorbyl Palmitate, Niacinamide, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200).
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INGREDIENTS AND APPEARANCE
BERKLEY JENSON ANTIBACTERIAL HAND
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68391-151 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERIN (UNII: PDC6A3C0OX) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) (UNII: X70SE62ZAR) ALOE VERA LEAF (UNII: ZY81Z83H0X) POLOXAMER 124 (UNII: 1S66E28KXA) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y) EDETATE SODIUM (UNII: MP1J8420LU) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM CITRATE (UNII: 1Q73Q2JULR) GREEN TEA LEAF (UNII: W2ZU1RY8B0) SACCHAROMYCES LYSATE (UNII: R85W246Z1C) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) ASCORBYL PALMITATE (UNII: QN83US2B0N) NIACINAMIDE (UNII: 25X51I8RD4) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68391-151-64 1892 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/16/2020 Labeler - BJWC (159082692) Registrant - Apollo Health and Beauty Care Inc. (201901209) Establishment Name Address ID/FEI Business Operations Apollo Health and Beauty Care Inc. 201901209 manufacture(68391-151)