Label: SHOPPING ANNUITY PREMIUM ANTI-BACTERIAL HANDSOAP- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 76209-118-08 - Packager: Market America, Inc.
- 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 March 12, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Use
- Warnings
- Directions
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Inactive ingredients
Water, Lauramine Oxide, Glycerin, Cocamidopropyl Betaine, Cetrimonium Chloride, PEG-120 Methyl Glucose Dioleate, PEG/PPG-120/10 Trimethylolpropane Trioleate, Laureth-2, Cocamide MEA, Citric Acid, Aloe Barbadensis Leaf Extract, Allantoin, Disodium EDTA, Sodium Chloride, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Magnesium Chloride, Magnesium Nitrate.
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SPL UNCLASSIFIED SECTION
CONVERT SPENDING INTO EARNING
TOUGH ON GERMS AND BACTERIA
HELPS TO ELIMINATE GERMS AND BACTERIA WITHOUT HARSH FRAGRANCES, ARTIFICIAL COLORS OR ALCOHOL
Manufactured for and distributed by:
Market America, Inc., 1302 Pleasant Ridge Road,
Greensboro, NC 27409, USAResale on third-party websites is strictly prohibited unless specifically authorized by Market America or its corporate affiliates. If barcodes are altered or you purchase this product from an unauthorized third-party website, the product is not guaranteed by Market America or its corporate affiliates.
- Packaging
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INGREDIENTS AND APPEARANCE
SHOPPING ANNUITY PREMIUM ANTI-BACTERIAL HANDSOAP
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76209-118 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) TRIMETHYLOLPROPANE TRIOLEATE (UNII: S448BZW2BR) LAURETH-2 (UNII: D4D38LT1L5) COCO MONOETHANOLAMIDE (UNII: C80684146D) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALLANTOIN (UNII: 344S277G0Z) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SODIUM CHLORIDE (UNII: 451W47IQ8X) EDETATE SODIUM (UNII: MP1J8420LU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) MAGNESIUM NITRATE (UNII: 77CBG3UN78) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76209-118-08 236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/11/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/11/2021 Labeler - Market America, Inc. (797412236) Registrant - Cemi International, Inc (015038336) Establishment Name Address ID/FEI Business Operations Cemi International, Inc 015038336 manufacture(76209-118)
