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AMOLG A

Medically reviewed by Drugs.com. Last updated on Mar 5, 2021.

Dosage form: cream
Ingredients: BETAMETHASONE VALERATE 0.61mg in 1g, GENTAMICIN SULFATE 1mg in 1g
Labeler: OASIS TRADING
NDC Code: 72689-0033

Betamethasone Valerate 0.61mg/g
Gentamicin Sulfate 1mg/g

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 affected area not more than 3 to 4 times daily

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 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

AMOLG A 
betamethasone valerate, gentamicin sulfate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72689-0033
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BETAMETHASONE VALERATE (BETAMETHASONE) BETAMETHASONE VALERATE0.61 mg  in 1 g
GENTAMICIN SULFATE (GENTAMICIN) GENTAMICIN1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL 
CETOSTEARYL ALCOHOL 
Packaging
#Item CodePackage Description
1NDC:72689-0033-135 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/15/2018
Labeler - OASIS TRADING (689991468)
Registrant - OASIS TRADING (689991468)
Establishment
NameAddressID/FEIOperations
OASIS TRADING689991468manufacture(72689-0033)

 
OASIS TRADING

Further information

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