PROHEAL TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment 
Nantong Health & Beyond Hygienic Products Inc.

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43473-067, PROHEAL tri antibiotics

Active Ingredients (in each gram)

Bacitracin zinc (bacitracin 400 units)
Neomycin sulfate (neomycin 3.5 mg)
Polymyxin B sulfate (polymyxin B 5.000 units

Purpose

First aid antibiotic

First aid antibiotic

First aid antibiotic

Uses

First aid to help prevent infection in minor cuts, scrapes and burns

Warnings

For external use only.

Do not use

  • in the eyes 
  • over large areas of the body
  • if you are allergic to any of the ingredients
  • longer than 1 week unless directed by a doctor.

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

  • if the condition persists or gets worse
  • a rash or other allergic reaction develops.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • Clean and disinfect the affected area
  • Apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily
  • May be covered with a sterile bandage.

Other Information

Store at room temperature

Inactive Ingredients

Mineral oil, petrolatum, purified water

image description

PROHEAL TRIPLE ANTIBIOTIC 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43473-067
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 [USP'U]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN0.0035 g  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 [USP'U]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
WATER (UNII: 059QF0KO0R)  
MINERAL OIL (UNII: T5L8T28FGP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43473-067-010.9 g in 1 PACKET; Type 0: Not a Combination Product01/17/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00401/17/2025
Labeler - Nantong Health & Beyond Hygienic Products Inc. (421280161)
Registrant - Nantong Health & Beyond Hygienic Products Inc. (421280161)
Establishment
NameAddressID/FEIBusiness Operations
Nantong Health & Beyond Hygienic Products Inc.421280161manufacture(43473-067)

Revised: 1/2025
 
Nantong Health & Beyond Hygienic Products Inc.