Head & Shoulders Conditioner

   
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Head & Shoulders Conditioner


Drug - Head & Shoulders Conditioner
The trade name of the product as shown on the labeling.

Dosage - LOTION; TOPICAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Pyrithione Zinc
Multiple ingredients are in alphabetical order.

Strength - 0.3%
The potency of the active ingredient(s), Pyrithione Zinc. May repeat for multiple part products.

Applicant - PROCTER AND GAMBLE
The firm name holding legal responsibility for Head & Shoulders Conditioner. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 019412
The FDA assigned number to Head & Shoulders Conditioner. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Head & Shoulders Conditioner. 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 - Mar 10, 1986
The date Head & Shoulders Conditioner 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) - No
The pioneer or innovator of Head & Shoulders Conditioner. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - DISCN
The group or category of approved drugs Head & Shoulders Conditioner is in. Format is RX, OTC, DISCN.

Applicant Full Name - Procter And Gamble Co
The full name of the firm holding legal responsibility for the new application of Head & Shoulders Conditioner.

Head & Shoulders Conditioner