CLINIQUE - 49527-112-01 - (OCTISALATE, AVOBENZONE, and OCTOCRYLENE)

Alphabetical Index


Drug Information of CLINIQUE

Product NDC: 49527-112
Proprietary Name: CLINIQUE
Non Proprietary Name: OCTISALATE, AVOBENZONE, and OCTOCRYLENE
Active Ingredient(s): 3; 5; 2.7    mL/100mL; mL/100mL; mL/100mL & nbsp;   OCTISALATE, AVOBENZONE, and OCTOCRYLENE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of CLINIQUE

Product NDC: 49527-112
Labeler Name: CLINIQUE LABORATORIES INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20111101

Package Information of CLINIQUE

Package NDC: 49527-112-01
Package Description: 1 TUBE in 1 CARTON (49527-112-01) > 50 mL in 1 TUBE

NDC Information of CLINIQUE

NDC Code 49527-112-01
Proprietary Name CLINIQUE
Package Description 1 TUBE in 1 CARTON (49527-112-01) > 50 mL in 1 TUBE
Product NDC 49527-112
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTISALATE, AVOBENZONE, and OCTOCRYLENE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20111101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name CLINIQUE LABORATORIES INC.
Substance Name AVOBENZONE; OCTISALATE; OCTOCRYLENE
Strength Number 3; 5; 2.7
Strength Unit mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of CLINIQUE


General Information