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Clearskin Professional - 10096-0185-2 - (OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE)

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Drug Information of Clearskin Professional

Product NDC: 10096-0185
Proprietary Name: Clearskin Professional
Non Proprietary Name: OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
Active Ingredient(s): 25; 71.1; 45; 30    mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Clearskin Professional

Product NDC: 10096-0185
Labeler Name: Avon Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20091221

Package Information of Clearskin Professional

Package NDC: 10096-0185-2
Package Description: 1 TUBE in 1 CARTON (10096-0185-2) > 75 mL in 1 TUBE (10096-0185-1)

NDC Information of Clearskin Professional

NDC Code 10096-0185-2
Proprietary Name Clearskin Professional
Package Description 1 TUBE in 1 CARTON (10096-0185-2) > 75 mL in 1 TUBE (10096-0185-1)
Product NDC 10096-0185
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20091221
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Avon Products, Inc.
Substance Name AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 25; 71.1; 45; 30
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL
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