Home > National Drug Code (NDC) > Alphaquin HP

Alphaquin HP - 58980-580-10 - (Hydroquinone, Octinoxate, and Oxybenzone)

Alphabetical Index


Drug Information of Alphaquin HP

Product NDC: 58980-580
Proprietary Name: Alphaquin HP
Non Proprietary Name: Hydroquinone, Octinoxate, and Oxybenzone
Active Ingredient(s): 40; 75; 50    mg/g; mg/g; mg/g & nbsp;   Hydroquinone, Octinoxate, and Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Alphaquin HP

Product NDC: 58980-580
Labeler Name: Stratus Pharamceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19930101

Package Information of Alphaquin HP

Package NDC: 58980-580-10
Package Description: 1 TUBE in 1 BOX (58980-580-10) > 28.4 g in 1 TUBE

NDC Information of Alphaquin HP

NDC Code 58980-580-10
Proprietary Name Alphaquin HP
Package Description 1 TUBE in 1 BOX (58980-580-10) > 28.4 g in 1 TUBE
Product NDC 58980-580
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroquinone, Octinoxate, and Oxybenzone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19930101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Stratus Pharamceuticals
Substance Name HYDROQUINONE; OCTINOXATE; OXYBENZONE
Strength Number 40; 75; 50
Strength Unit mg/g; mg/g; mg/g
Pharmaceutical Classes Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA]

Complete Information of Alphaquin HP


General Information