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Moisture Therapy - 10096-0249-1 - (OCTINOXATE, OCTISALATE, OXYBENZONE)

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Drug Information of Moisture Therapy

Product NDC: 10096-0249
Proprietary Name: Moisture Therapy
Non Proprietary Name: OCTINOXATE, OCTISALATE, OXYBENZONE
Active Ingredient(s): 75; 50; 10    mg/mL; mg/mL; mg/mL & nbsp;   OCTINOXATE, OCTISALATE, OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Moisture Therapy

Product NDC: 10096-0249
Labeler Name: Avon Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110411

Package Information of Moisture Therapy

Package NDC: 10096-0249-1
Package Description: 400 mL in 1 BOTTLE (10096-0249-1)

NDC Information of Moisture Therapy

NDC Code 10096-0249-1
Proprietary Name Moisture Therapy
Package Description 400 mL in 1 BOTTLE (10096-0249-1)
Product NDC 10096-0249
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OCTISALATE, OXYBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110411
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Avon Products, Inc.
Substance Name OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 75; 50; 10
Strength Unit mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Moisture Therapy


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