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Publix Baby - 56062-704-16 - (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE)

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Drug Information of Publix Baby

Product NDC: 56062-704
Proprietary Name: Publix Baby
Non Proprietary Name: AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Active Ingredient(s): 3; 13; 5; 7; 4    g/100g; g/100g; g/100g; g/100g; g/100g & nbsp;   AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Publix Baby

Product NDC: 56062-704
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121115

Package Information of Publix Baby

Package NDC: 56062-704-16
Package Description: 226 g in 1 BOTTLE, PLASTIC (56062-704-16)

NDC Information of Publix Baby

NDC Code 56062-704-16
Proprietary Name Publix Baby
Package Description 226 g in 1 BOTTLE, PLASTIC (56062-704-16)
Product NDC 56062-704
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20121115
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Publix Super Markets Inc
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 Publix Baby


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