Label: ANTIBACTERIAL BANDAGES- benzalkonium chloride dressing
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NDC Code(s):
71584-0111-1,
71584-0111-2,
71584-0111-3,
71584-0111-4, view more71584-0111-5, 71584-0111-6, 71584-0111-7, 71584-0111-8
- Packager: Guangdong Comfort Medical Products Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 26, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- Purpose
- USE
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WARNINGS
For external use only.
Stop use and consult a doctor if the condition persists or gets worse.
Do not use longer than 1 week unless directed by a physician. In case of deep or puncture wounds, animal bites, or serious burn, consult a physician.
Keep out of reach of children. if swallowed get medical help or contact Poison control Center right away.
- Other Information
- DIRECTIONS
- INACTIVE INGREDIENT
- Keep out of reach of children
- Dosage and administration
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Label principal display panel
NDC 71584-0111-1
ANTIBACTERIAL BANDAGES
Drug Facts
ACTIVE INGREDIENTS
Benzalkonium Chloride 0.13%Purpose
AntisepticUSE
First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.WARNINGS For external use only.
Stop use and consult a doctor if the condition persists or gets worse.
Do not use
longer than one week unless directed by a physician. In case of deep or puncture wounds, animal bites, or serious burn, consult a physician.Keep out of reach of children. if swallowed get medical help or contact Poison control Center right away.
DIRECTIONS
Clean and dry the affected area. Apply a sterile bandage on the area 1 to 3 times daily.Other Information: not intended for use on delicate or sensitive skin.
INACTIVE INGREDIENT
Water
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL BANDAGES
benzalkonium chloride dressingProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71584-0111 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 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71584-0111-1 0.5 g in 1 POUCH; Type 0: Not a Combination Product 10/15/2021 2 NDC:71584-0111-2 0.5 g in 1 POUCH; Type 0: Not a Combination Product 10/15/2021 3 NDC:71584-0111-3 0.5 g in 1 POUCH; Type 0: Not a Combination Product 10/15/2021 4 NDC:71584-0111-4 0.5 g in 1 POUCH; Type 0: Not a Combination Product 10/15/2021 5 NDC:71584-0111-5 0.5 g in 1 POUCH; Type 0: Not a Combination Product 10/15/2021 6 NDC:71584-0111-6 0.5 g in 1 POUCH; Type 0: Not a Combination Product 10/15/2021 7 NDC:71584-0111-7 0.578 g in 1 POUCH; Type 0: Not a Combination Product 09/22/2022 8 NDC:71584-0111-8 1.29 g in 1 POUCH; Type 0: Not a Combination Product 09/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 10/15/2021 Labeler - Guangdong Comfort Medical Products Co., Ltd. (544507534) Registrant - Guangdong Comfort Medical Products Co., Ltd. (544507534) Establishment Name Address ID/FEI Business Operations Guangdong Comfort Medical Products Co., Ltd. 544507534 manufacture(71584-0111)