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Hydroquinone - 68788-9916-2 - (HYDROQUINONE, DIOXYBENZONE, OXYBENZONE, PADIMATE O)

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Drug Information of Hydroquinone

Product NDC: 68788-9916
Proprietary Name: Hydroquinone
Non Proprietary Name: HYDROQUINONE, DIOXYBENZONE, OXYBENZONE, PADIMATE O
Active Ingredient(s): 30; 40; 20; 80    mg/g; mg/g; mg/g; mg/g & nbsp;   HYDROQUINONE, DIOXYBENZONE, OXYBENZONE, PADIMATE O
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroquinone

Product NDC: 68788-9916
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120130

Package Information of Hydroquinone

Package NDC: 68788-9916-2
Package Description: 1 TUBE in 1 CARTON (68788-9916-2) > 28.35 g in 1 TUBE

NDC Information of Hydroquinone

NDC Code 68788-9916-2
Proprietary Name Hydroquinone
Package Description 1 TUBE in 1 CARTON (68788-9916-2) > 28.35 g in 1 TUBE
Product NDC 68788-9916
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROQUINONE, DIOXYBENZONE, OXYBENZONE, PADIMATE O
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120130
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name DIOXYBENZONE; HYDROQUINONE; OXYBENZONE; PADIMATE O
Strength Number 30; 40; 20; 80
Strength Unit mg/g; mg/g; mg/g; mg/g
Pharmaceutical Classes Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA]

Complete Information of Hydroquinone


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