Label: BANDAGE- benzalkonium chloride swab
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Contains inactivated NDC Code(s)
NDC Code(s): 69119-001-01, 69119-001-02, 69119-001-03 - Packager: Dongyang Haodi Medical CO.,Ltd
- 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 July 24, 2014
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- Active Ingredients
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INGREDIENTS AND APPEARANCE
BANDAGE
benzalkonium chloride swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69119-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.0012 mg in 1 mg Inactive Ingredients Ingredient Name Strength COTTON FIBER (UNII: 70LDW53ROO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69119-001-02 36 in 1 CARTON 1 40 in 1 BOX 1 0.0459 mg in 1 POUCH 2 NDC:69119-001-01 24 in 1 CARTON 2 40 in 1 BOX 2 0.0459 mg in 1 POUCH 3 NDC:69119-001-03 12 in 1 CARTON 3 40 in 1 BOX 3 0.0459 mg in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/16/2014 Labeler - Dongyang Haodi Medical CO.,Ltd (421361763) Establishment Name Address ID/FEI Business Operations Dongyang Haodi Medical CO.,Ltd 421361763 manufacture(69119-001)