Lidocaine and Hydrocortisone Cream

Name: Lidocaine and Hydrocortisone Cream

Inactive ingredients

ALUMINUM SULFATE, CALCIUM ACETATE, CETYL ALCOHOL, METHYLPARABEN, MINERAL OIL, POLYSORBATE 60, PROPYLENE GLYCOL, PROPYLPARABEN, PURIFIED WATER, SODIUM HYDROXIDE, SORBITAN STEARATE, STEARIC ACID, STEARYL ALCOHOL.

Nursing mothers

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when this drug is administered to a nursing mother.

Keep this and all medications out of reach of children.

Store at 20°-25°C (68°-77°F) [see USP Controlled Temperature].

Protect from freezing.

Caton (1 oz)

Carton (14 pc KIT)

Carton (20 pc KIT)

LIDOCAINE HCL - HYDROCORTISONE ACETATE 
lidocaine hcl and hydrocortisone acetate cream
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:59088-819
Route of Administration TOPICAL, RECTAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE HYDROCHLORIDE ANHYDROUS 30 mg  in 1 g
HYDROCORTISONE ACETATE (HYDROCORTISONE) HYDROCORTISONE ACETATE 5 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
ALUMINUM SULFATE  
CALCIUM ACETATE  
CETYL ALCOHOL  
METHYLPARABEN  
MINERAL OIL  
POLYSORBATE 60  
PROPANEDIOL  
PROPYLPARABEN  
WATER  
SODIUM HYDROXIDE  
SORBITAN MONOSTEARATE  
STEARIC ACID  
STEARYL ALCOHOL  
Packaging
# Item Code Package Description
1 NDC:59088-819-14 14 TUBE in 1 KIT
1 NDC:59088-819-01 7 g in 1 TUBE
2 NDC:59088-819-03 1 TUBE in 1 CARTON
2 28.3 g in 1 TUBE
3 NDC:59088-819-07 1 TUBE in 1 CARTON
3 85 g in 1 TUBE
4 NDC:59088-819-20 20 TUBE in 1 KIT
4 NDC:59088-819-01 7 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 07/01/2011
Labeler - PureTek Corporation (785961046)
Revised: 01/2017   PureTek Corporation
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