sunscreen - 19392-400-04 - (octinoxate, octisalate, octocrylene, oxybenzone)

Alphabetical Index


Drug Information of sunscreen

Product NDC: 19392-400
Proprietary Name: sunscreen
Non Proprietary Name: octinoxate, octisalate, octocrylene, oxybenzone
Active Ingredient(s): 65; 40; 70; 55    mg/g; mg/g; mg/g; mg/g & nbsp;   octinoxate, octisalate, octocrylene, oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of sunscreen

Product NDC: 19392-400
Labeler Name: Humphreyline
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100101

Package Information of sunscreen

Package NDC: 19392-400-04
Package Description: 44 g in 1 BOTTLE, PLASTIC (19392-400-04)

NDC Information of sunscreen

NDC Code 19392-400-04
Proprietary Name sunscreen
Package Description 44 g in 1 BOTTLE, PLASTIC (19392-400-04)
Product NDC 19392-400
Product Type Name HUMAN OTC DRUG
Non Proprietary Name octinoxate, octisalate, octocrylene, oxybenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20100101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Humphreyline
Substance Name OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 65; 40; 70; 55
Strength Unit mg/g; mg/g; mg/g; mg/g
Pharmaceutical Classes

Complete Information of sunscreen


General Information