MADECASSOL (ointment) I World Pharmaceutical Co., Ltd. Skip to main content

MADECASSOL

Dosage form: ointment
Ingredients: CENTELLA ASIATICA 10mg in 1g, NEOMYCIN SULFATE 3.5mg in 1g
Labeler: I World Pharmaceutical Co., Ltd.
NDC code: 73442-0004

Medically reviewed by Drugs.com. Last updated on Oct 30, 2023.

Neomycin Sulfate, Titrated Ext. of Centella Asiatica

■ temporary relief of itching associated with minor skin irritations and rashes due to eczema, insect bites, poison ivy, poison oak, or poison sumac soaps detergents, cosmetics, jewelry, seborrheic dermatitis, psoriasis, external genital and anal itching

Keep out of reach of children

■ Adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily

For external use only.

Do not use in the eyes by putting this product into the rectum by using fingers or any mechanical device or applicator.

Ask a doctor before use if you have a vaginal discharge, rectal bleeding, diaper rash.

When using this product consult a doctor before exceeding recommended dosage.

Stop use and ask a doctor if condition gets worse, condition persists for more than 7 days, condition clears up and occurs again with within a few days. Do not begin to use any other hydrocortisone product unless you have consulted a doctor.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

cetostearyl alcohol, propylene glycol, purified water, sodium lauryl sulfate, white petrolatum

For external use only

MADECASSOL 
neomycin sulfate, titrated ext. of centella asiatica ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73442-0004
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CENTELLA ASIATICA (CENTELLA ASIATICA) CENTELLA ASIATICA10 mg  in 1 g
NEOMYCIN SULFATE (NEOMYCIN) NEOMYCIN SULFATE3.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL 
CETOSTEARYL ALCOHOL 
PETROLATUM 
Packaging
#Item CodePackage Description
1NDC:73442-0004-110 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/08/2019
Labeler - I World Pharmaceutical Co., Ltd. (688222857)
Registrant - I World Pharmaceutical Co., Ltd. (688222857)
Establishment
NameAddressID/FEIOperations
I World Pharmaceutical Co., Ltd688222857manufacture(73442-0004)

 
I World Pharmaceutical Co., Ltd.

Further information

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