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OHUI SUN SCIENCE Perfect Sunblock Blue EX plus - 53208-539-02 - (TITANIUM DIOXIDE, OCTOCRYLENE, POLYSILICONE-15, OCTISALATE, ENSULIZOLE, BEMOTRIZINOL)

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Drug Information of OHUI SUN SCIENCE Perfect Sunblock Blue EX plus

Product NDC: 53208-539
Proprietary Name: OHUI SUN SCIENCE Perfect Sunblock Blue EX plus
Non Proprietary Name: TITANIUM DIOXIDE, OCTOCRYLENE, POLYSILICONE-15, OCTISALATE, ENSULIZOLE, BEMOTRIZINOL
Active Ingredient(s): 2; 3.9; 4.8; 5; 9    mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   TITANIUM DIOXIDE, OCTOCRYLENE, POLYSILICONE-15, OCTISALATE, ENSULIZOLE, BEMOTRIZINOL
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of OHUI SUN SCIENCE Perfect Sunblock Blue EX plus

Product NDC: 53208-539
Labeler Name: LG Household and Healthcare, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110803

Package Information of OHUI SUN SCIENCE Perfect Sunblock Blue EX plus

Package NDC: 53208-539-02
Package Description: 1 CONTAINER in 1 BOX (53208-539-02) > 60 mL in 1 CONTAINER (53208-539-01)

NDC Information of OHUI SUN SCIENCE Perfect Sunblock Blue EX plus

NDC Code 53208-539-02
Proprietary Name OHUI SUN SCIENCE Perfect Sunblock Blue EX plus
Package Description 1 CONTAINER in 1 BOX (53208-539-02) > 60 mL in 1 CONTAINER (53208-539-01)
Product NDC 53208-539
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TITANIUM DIOXIDE, OCTOCRYLENE, POLYSILICONE-15, OCTISALATE, ENSULIZOLE, BEMOTRIZINOL
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110803
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name LG Household and Healthcare, Inc.
Substance Name BEMOTRIZINOL; ENSULIZOLE; OCTISALATE; POLYSILICONE-15; TITANIUM DIOXIDE
Strength Number 2; 3.9; 4.8; 5; 9
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of OHUI SUN SCIENCE Perfect Sunblock Blue EX plus


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