Label: BAC-D ANTIBACTERIAL WOUND AND SKIN CARE- benzalkonium chloride spray
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Contains inactivated NDC Code(s)
NDC Code(s): 69082-500-16 - Packager: RDM Products, 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 November 10, 2015
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Keep out of reach of children.
- Uses
- Warnings
- Directions for use
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
BAC-D ANTIBACTERIAL WOUND AND SKIN CARE
benzalkonium chloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69082-500 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) UREA (UNII: 8W8T17847W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69082-500-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/12/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/12/2014 Labeler - RDM Products, Inc (034340230) Establishment Name Address ID/FEI Business Operations RDM Products, Inc 034340230 manufacture(69082-500)