FAMILY CARE ANTIBIOTIC PAIN RELIEF 0.33OZ- antibiotic pain relief cream

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients (in each gram) Purposes
Neomycin Sulfate (3.5 mg).......................................................First Aid Antibiotic
Polymyxin B Sulfate (10,000 units)...........................................First Aid Antibiotic
Pramoxine HCI (10 mg)............................................................External Analgesic

PURPOSE

Uses
first aid to help prevent infection and for the temporary relief of pain in minor:
 cuts  scrapes  burns

WARNINGS

Warnings
For external use only.

DO NOT USE

Do not use
 in the eyes
 over large areas of the body
 if you are allergic to any of the ingredients

WHEN USING

Ask a doctor before use if you have
 deep or puncture wounds
 animal bites
 serious burns

STOP USE

Stop use and ask a doctor if
 condition persists or gets worse
 rash or other allergic reaction develops
 you need to use longer than 1 week

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a
Poison Control Center (1-800-222-1222) right away.

INDICATIONS & USAGE

Directions
 adults and children 2 years of age and older:
 clean 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
 children 2 years or younger: consult with a doctor

STORAGE AND HANDLING

Other information
 store at 20° to 25°C (68° to 77°F)

INACTIVE INGREDIENT

Inactive ingredients
butylated hydroxytoluene, cetyl alcohol, light mineral oil, methylparaben,
petrolatum, polysorbate 60, propylene glycol, propylparaben, purified water,
sorbitan monostearate, stearic acid

DOSAGE & ADMINISTRATION

Questions or comments?
Call 1-888-645-8204 Monday-Friday 9AM-5PM (PST)
*This product is not manufactured or distributed by Kenvue Brands LLC
distributor of Neosporin® + Pain Relief Cream.
Distributed by: UNITED EXCHANGE CORP.
Cypress, CA 90630 USA | 1-888-645-8204
Made in China
689-ZDP-BX-R1
OM-TP-ZDP311-R1

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FAMILY CARE ANTIBIOTIC PAIN RELIEF 0.33OZ 
antibiotic pain relief cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-578
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg  in 1 g
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

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 60 (UNII: CAL22UVI4M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CETYL ALCOHOL (UNII: 936JST6JCN)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
STEARIC ACID (UNII: 4ELV7Z65AP)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-578-33	1 in 1 BOX	04/15/2026
1		1 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	M017	04/15/2026

Labeler - United Exchange Corp (840130579)