Label: BCP- benzalkonium chloride cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 78502-5000-5 - Packager: BELSKIN S. DE, R.L. DE C.V
- 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 May 27, 2020
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- Official Label (Printer Friendly)
- CLEANING, DISINFECTIN AND STERILIZATION INSTRUCTIONS
- ENVIRONMENTAL WARNING
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS AND PRECAUTIONS
- DOSAGE AND ADMINISTRATION
- INACTIVE INGREDIENTS
- ACTIVE INGREDIENT
- INDICATIONS AND USAGE
- PURPOSE
- WARNINGS
- PACKAGE LABEL
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INGREDIENTS AND APPEARANCE
BCP
benzalkonium chloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78502-5000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.0025 g in 1 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF POLYSACCHARIDES (UNII: W21O437517) 0.05 g in 1 g GLYCERIN (UNII: PDC6A3C0OX) 0.05 g in 1 g DIMETHICONE (UNII: 92RU3N3Y1O) 0.005 g in 1 g CITRIC ACID ACETATE (UNII: DSO12WL7AU) 0.015 g in 1 g MINERAL OIL (UNII: T5L8T28FGP) 0.01 g in 1 g WATER (UNII: 059QF0KO0R) 0.8675 g in 1 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78502-5000-5 40 g in 1 BAG; Type 0: Not a Combination Product 05/27/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/27/2020 Labeler - BELSKIN S. DE, R.L. DE C.V (816649743) Registrant - BELSKIN S. DE, R.L. DE C.V (816649743) Establishment Name Address ID/FEI Business Operations BELSKIN S. DE, R.L. DE C.V 816649743 manufacture(78502-5000)