Home > National Drug Code (NDC) > Moisturizer

Moisturizer - 41250-820-26 - (octinoxate, octisalate, oxybenzone)

Alphabetical Index


Drug Information of Moisturizer

Product NDC: 41250-820
Proprietary Name: Moisturizer
Non Proprietary Name: octinoxate, octisalate, oxybenzone
Active Ingredient(s): 8.86; 5.9; 3.54    mL/118mL; mL/118mL; mL/118mL & nbsp;   octinoxate, octisalate, oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Moisturizer

Product NDC: 41250-820
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20090504

Package Information of Moisturizer

Package NDC: 41250-820-26
Package Description: 1 BOTTLE in 1 CARTON (41250-820-26) > 118 mL in 1 BOTTLE

NDC Information of Moisturizer

NDC Code 41250-820-26
Proprietary Name Moisturizer
Package Description 1 BOTTLE in 1 CARTON (41250-820-26) > 118 mL in 1 BOTTLE
Product NDC 41250-820
Product Type Name HUMAN OTC DRUG
Non Proprietary Name octinoxate, octisalate, oxybenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20090504
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Meijer Distribution Inc
Substance Name OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 8.86; 5.9; 3.54
Strength Unit mL/118mL; mL/118mL; mL/118mL
Pharmaceutical Classes

Complete Information of Moisturizer


General Information