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ReCellTis

Medically reviewed by Drugs.com. Last updated on Mar 11, 2021.

Dosage form: cream
Ingredients: BACITRACIN ZINC 400[USP'U] in 1g, NEOMYCIN SULFATE 3.5mg in 1g, POLYMYXIN B SULFATE 5000[USP'U] in 1g, LIDOCAINE 20mg in 1g
Labeler: CellNovation Technology Corporation
NDC Code: 71929-069

ReCellTis

ReCellTis +Pain & Itch Relief First Aid Cream

Drug Facts

Active Ingredients (in each gram)

Bacitracin Zinc 400 units

Neomycin Sulfate 5mg (equivalent to 3.5 mg of neomycin base)

Polymyxin B Sulfate 5,000 units

Lidocaine Hydrochloride 20 mg

Purpose

First aid antibiotic

First aid antibiotic

First aid antibiotic

Local anesthetic

Uses

First aid to prevent infection, for temporary relief of pain or discomfort, and helps promote skin repair in minor:

  • Cuts
  • Scrapes
  • Burns

Warnings

For external use only

Do not use
  • in the eyes
  • if you are allergic to any of the ingredients
  • over 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

  • you need to use longer than 1 week
  • rash or other allergic reaction develops
  • condition persists or gets worse

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Adults and children 2 years of age or older:

  • clean the affected area
  • apply a small amount (thin layer) on the area 1 to 3 times daily
  • may be covered with sterile bandage

Children under 2 years of age: ask a doctor

Other Information
  • store at 15° to 30°C (59° to 86°F)
  • protect from freezing and avoid excessive heat

Inactive ingredients

Carboxymethyl Cellulose, Cetostearyl Alcohol, Cetyl Alcohol, CoEnzyme Q-10, Purified Water, Phenoxyethanol, Polysorbate 80, Sorbitan Oleate, Tocopheryl Acetate , White Petrolatum, Zinc Gluconate.

PRINCIPAL DISPLAY PANEL

RECELLTIS 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, lidocaine hcl cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71929-069
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (BACITRACIN) BACITRACIN400 [USP'U]  in 1 g
NEOMYCIN SULFATE (NEOMYCIN) NEOMYCIN3.5 mg  in 1 g
POLYMYXIN B SULFATE (POLYMYXIN B) POLYMYXIN B5000 [USP'U]  in 1 g
LIDOCAINE (LIDOCAINE) LIDOCAINE20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
COENZYME Q10, (2Z)- 
POLYSORBATE 80 
PETROLATUM 
CETOSTEARYL ALCOHOL 
CARBOXYMETHYLCELLULOSE 
WATER 
PHENOXYETHANOL 
PEG-6 SORBITAN OLEATE 
ALPHA-TOCOPHEROL ACETATE 
ZINC GLUCONATE 
CETYL ALCOHOL 
Packaging
#Item CodePackage Description
1NDC:71929-069-3228 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B03/21/2018
Labeler - CellNovation Technology Corporation (080976562)

 
CellNovation Technology Corporation

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

More about bacitracin / lidocaine / neomycin / polymyxin b topical