FAMILY WELLNESS PLUS PAIN RELIEF- family wellness neomycin,polymyxinb,pramoxinehcl cream 
Trifecta Pharmaceutical USA LLC

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.

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Triple Antibiotic + Pain Relief Cream

DRUG FACTS

Active Ingredient

Neomycin 3.5mg

Purpose

First Aid Antibiotic

Active Ingredient

Polymyxin B 10,000 Units

Purpose

First Aid Antibiotic

Active Ingredient

Pramoxine HCL 10mg

Purpose

External Analgesic

Uses

First Aid to help prevent infection in minor:

Warnings

For external use only. Do not use:

Ask a Doctor before Use

Ask Doctor before use if you have:

Stop Use and ask a Doctor if:

Keep out of Reach of Children

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

Directions

Other Information

Inactive Ingredient:

Cetostearyl alcohol, Ethylparaben, Glycerin, Glyceryl Sterate, Levelling Agent O, Light Mineral Oil, Petrolatum, Purified Water, Sodium Dodecyl Sulfate.

Questions?

Call 1-888-296-9067

Weekdays 9AM - 4PM EST

DISTRIBUTED BY: MIDWOOD BRANDS, LLC.

500 Volvo Parkway, Chesapeake, VA. 23320

NOT SATISFIED?

Return package and unused product within 30 days to any Family Dollar store for a refund (with receipt) or exchange.

This product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the registered trademark Neosporin® Plus Pain Relief.

MADE IN CHINA

Packaging

triple antibiotic plus pain 3

FAMILY WELLNESS PLUS PAIN RELIEF 
family wellness neomycin,polymyxinb,pramoxinehcl cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69396-043
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE3.5 mg  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1 g
Inactive Ingredients
Ingredient NameStrength
LAURYL ALCOHOL (UNII: 178A96NLP2)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
PETROLATUM (UNII: 4T6H12BN9U)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
WATER (UNII: 059QF0KO0R)  
ETHYLPARABEN (UNII: 14255EXE39)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69396-043-011 in 1 BOX09/22/2019
128.4 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B08/30/2019
Labeler - Trifecta Pharmaceutical USA LLC (079424163)

Revised: 12/2019
Document Id: 98fac7f9-0d41-8da5-e053-2995a90a8390
Set id: 9350688e-f456-d9e5-e053-2995a90aa8bb
Version: 4
Effective Time: 20191205
 
Trifecta Pharmaceutical USA LLC