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Sun protection body - 76157-511-02 - (Avobenzone, Homosalate, Octislate, Oxybenzone)

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Drug Information of Sun protection body

Product NDC: 76157-511
Proprietary Name: Sun protection body
Non Proprietary Name: Avobenzone, Homosalate, Octislate, Oxybenzone
Active Ingredient(s): 3; 7; 5    mL/100mL; mL/100mL; mL/100mL & nbsp;   Avobenzone, Homosalate, Octislate, Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sun protection body

Product NDC: 76157-511
Labeler Name: La Prairie Group AG
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110214

Package Information of Sun protection body

Package NDC: 76157-511-02
Package Description: 1 BOTTLE in 1 BOX (76157-511-02) > 180 mL in 1 BOTTLE (76157-511-01)

NDC Information of Sun protection body

NDC Code 76157-511-02
Proprietary Name Sun protection body
Package Description 1 BOTTLE in 1 BOX (76157-511-02) > 180 mL in 1 BOTTLE (76157-511-01)
Product NDC 76157-511
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Homosalate, Octislate, Oxybenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110214
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name La Prairie Group AG
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE
Strength Number 3; 7; 5
Strength Unit mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Sun protection body


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