Home > National Drug Code (NDC) > GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN

GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN - 52456-018-50 - (HOMOSALATE, OCTINOXATE, OXYBENZONE)

Alphabetical Index


Drug Information of GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN

Product NDC: 52456-018
Proprietary Name: GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN
Non Proprietary Name: HOMOSALATE, OCTINOXATE, OXYBENZONE
Active Ingredient(s): 3; 8; 2    mL/100mL; mL/100mL; mL/100mL & nbsp;   HOMOSALATE, OCTINOXATE, OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN

Product NDC: 52456-018
Labeler Name: Rodial, Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100630

Package Information of GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN

Package NDC: 52456-018-50
Package Description: 1 BOTTLE in 1 BOX (52456-018-50) > 50 mL in 1 BOTTLE

NDC Information of GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN

NDC Code 52456-018-50
Proprietary Name GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN
Package Description 1 BOTTLE in 1 BOX (52456-018-50) > 50 mL in 1 BOTTLE
Product NDC 52456-018
Product Type Name HUMAN OTC DRUG
Non Proprietary Name HOMOSALATE, OCTINOXATE, OXYBENZONE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20100630
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rodial, Ltd.
Substance Name HOMOSALATE; OCTINOXATE; OXYBENZONE
Strength Number 3; 8; 2
Strength Unit mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN


General Information