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Walgreens Sunscreen Baby - 0363-4010-22 - (HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE)

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Drug Information of Walgreens Sunscreen Baby

Product NDC: 0363-4010
Proprietary Name: Walgreens Sunscreen Baby
Non Proprietary Name: HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE
Active Ingredient(s): 3; 13; 5; 7; 4    g/100g; g/100g; g/100g; g/100g; g/100g & nbsp;   HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Walgreens Sunscreen Baby

Product NDC: 0363-4010
Labeler Name: WALGREEN CO.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121204

Package Information of Walgreens Sunscreen Baby

Package NDC: 0363-4010-22
Package Description: 85 g in 1 BOTTLE, PLASTIC (0363-4010-22)

NDC Information of Walgreens Sunscreen Baby

NDC Code 0363-4010-22
Proprietary Name Walgreens Sunscreen Baby
Package Description 85 g in 1 BOTTLE, PLASTIC (0363-4010-22)
Product NDC 0363-4010
Product Type Name HUMAN OTC DRUG
Non Proprietary Name HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20121204
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name WALGREEN CO.
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 3; 13; 5; 7; 4
Strength Unit g/100g; g/100g; g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of Walgreens Sunscreen Baby


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