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MOISTURISING SUN PROTECTION - 76450-050-01 - (OCTINOXATE)

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Drug Information of MOISTURISING SUN PROTECTION

Product NDC: 76450-050
Proprietary Name: MOISTURISING SUN PROTECTION
Non Proprietary Name: OCTINOXATE
Active Ingredient(s): 1.5; 1; 1.5; 3    mL/50mL; mL/50mL; mL/50mL; mL/50mL & nbsp;   OCTINOXATE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of MOISTURISING SUN PROTECTION

Product NDC: 76450-050
Labeler Name: Mesoestetic, S.L.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120201

Package Information of MOISTURISING SUN PROTECTION

Package NDC: 76450-050-01
Package Description: 50 mL in 1 TUBE (76450-050-01)

NDC Information of MOISTURISING SUN PROTECTION

NDC Code 76450-050-01
Proprietary Name MOISTURISING SUN PROTECTION
Package Description 50 mL in 1 TUBE (76450-050-01)
Product NDC 76450-050
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Mesoestetic, S.L.
Substance Name AVOBENZONE; ENSULIZOLE; ENZACAMENE; OCTINOXATE
Strength Number 1.5; 1; 1.5; 3
Strength Unit mL/50mL; mL/50mL; mL/50mL; mL/50mL
Pharmaceutical Classes

Complete Information of MOISTURISING SUN PROTECTION


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