E-z Scrub 241
Drug - E-z Scrub 241
The trade name of the product as shown on the labeling.
Dosage -
SPONGE; TOPICAL
The product dosage form and route separated by a semi-colon.
Active Ingredient(s) -
Povidone-iodine
Multiple ingredients are in alphabetical order.
Strength -
10%
The potency of the active ingredient(s), Povidone-iodine. May repeat for multiple part products.
Applicant -
BECTON DICKINSON
The firm name holding legal responsibility for E-z Scrub 241. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
019476
The FDA assigned number to E-z Scrub 241. Format is nnnnnn.
Product Number -
001
The FDA assigned number to identify E-z Scrub 241. Each strength is a separate product. May repeat for multiple part products. Format is nnn.
Therapeutic Equivalence (TE) Code -
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.
Approval Date -
Jan 7, 1987
The date E-z Scrub 241 was approved as stated in the FDA approval letter to the applicant. The format is Mmm dd, yyyy. Products approved prior to the January 1, 1982 contain the phrase: "Approved prior to Jan 1, 1982".
Reference Listed Drug (RLD) -
Yes
The pioneer or innovator of E-z Scrub 241. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.
Type -
OTC
The group or category of approved drugs E-z Scrub 241 is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Becton Dickinson And Co
The full name of the firm holding legal responsibility for the new application of E-z Scrub 241.
E-z Scrub 241
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