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VIALPROTECTION - 16555-006-01 - (HOMOSALATE, OCTISALATE, AVOBENZONE OXYBENZONE)

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Drug Information of VIALPROTECTION

Product NDC: 16555-006
Proprietary Name: VIALPROTECTION
Non Proprietary Name: HOMOSALATE, OCTISALATE, AVOBENZONE OXYBENZONE
Active Ingredient(s): 3; 5; 5; 3    mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   HOMOSALATE, OCTISALATE, AVOBENZONE OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of VIALPROTECTION

Product NDC: 16555-006
Labeler Name: DARPHIN DIST.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20090901

Package Information of VIALPROTECTION

Package NDC: 16555-006-01
Package Description: 1 TUBE in 1 CARTON (16555-006-01) > 50 mL in 1 TUBE (16555-006-02)

NDC Information of VIALPROTECTION

NDC Code 16555-006-01
Proprietary Name VIALPROTECTION
Package Description 1 TUBE in 1 CARTON (16555-006-01) > 50 mL in 1 TUBE (16555-006-02)
Product NDC 16555-006
Product Type Name HUMAN OTC DRUG
Non Proprietary Name HOMOSALATE, OCTISALATE, AVOBENZONE OXYBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20090901
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name DARPHIN DIST.
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE
Strength Number 3; 5; 5; 3
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of VIALPROTECTION


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