ANTIBIOTIC AND PAIN RELIEF- neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride cream

Antibiotic and Pain Relief by

Drug Labeling and Warnings

Antibiotic and Pain Relief by is a Otc medication manufactured, distributed, or labeled by Target Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts 

Active ingredients

Neomycin Sulfate (3.5mg) 
Polymixin B Sulfate (10,000 units) 
Pramoxine Hydrochloride (10 mg)

Purpose

First Aid Antibiotic
First Aid Antibiotic
External Analgesic

Uses

first aid to prevent infection and for the temporary relief of pain or discomfort in minor:

• cuts
• scapes
• burns

Warnings For external use only

Allergy alert

• do not use if you are allergic to any of the ingredients

Do not use

• in or near the eyes
• or on large areas of the body

Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

Stop use and ask a doctor if

• condition persists or gets worse
• symptoms last for more than 7 days or clear up and come back within a few days
• a rash or other allergic reaction develops

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children. If swallowed get medical help or contact a Poison Control Center immediately.

Directions 

• clean the affected area
• apply a small amount (equal to surface area of tip of finger) on the area 1 to 3 times daily.
• may be covered with a sterile bandage

Other inofrmation 

Store at a controlled room temperature 68º-77ºF (20º-25ºC)

Inactive ingredients 

Ceteareth-20, Cetearyl Alcohol, Glyceryl Stearate SE, Methylparaben, Mineral Oil, Phosphoric Acid, Propylene Glycol, Purified Water, White Petrolatum

Questions or comment? 1-800-910-6874

Principal Display Panel 

Target up&Up       NDC: 11673-770-14

Maximum Strength Pain Releiving & Infection Protection 

Neomycin Sulfate/ Polymyxin B Sulfate / Pramoxine HCL 

NET WT 0.5oz (14g)

INGREDIENTS AND APPEARANCE

ANTIBIOTIC AND PAIN RELIEF 
neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-770
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	10000 [USP'U]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN	3.5 mg  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
METHYLPARABEN (UNII: A2I8C7HI9T)
MINERAL OIL (UNII: T5L8T28FGP)
PHOSPHORIC ACID (UNII: E4GA8884NN)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-770-14	1 in 1 CARTON	01/31/2024
1		14 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	01/31/2024

Labeler - Target Corporation (006961700)