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moisturising sunscreen - 42315-672-02 - (Homosalate, Octisalate, Octinoxate, Octocrylene)

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Drug Information of moisturising sunscreen

Product NDC: 42315-672
Proprietary Name: moisturising sunscreen
Non Proprietary Name: Homosalate, Octisalate, Octinoxate, Octocrylene
Active Ingredient(s): 8; 3; 4    mL/100mL; mL/100mL; mL/100mL & nbsp;   Homosalate, Octisalate, Octinoxate, Octocrylene
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of moisturising sunscreen

Product NDC: 42315-672
Labeler Name: Eshu Pty Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110217

Package Information of moisturising sunscreen

Package NDC: 42315-672-02
Package Description: 1 BOTTLE in 1 BOX (42315-672-02) > 100 mL in 1 BOTTLE (42315-672-01)

NDC Information of moisturising sunscreen

NDC Code 42315-672-02
Proprietary Name moisturising sunscreen
Package Description 1 BOTTLE in 1 BOX (42315-672-02) > 100 mL in 1 BOTTLE (42315-672-01)
Product NDC 42315-672
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Homosalate, Octisalate, Octinoxate, Octocrylene
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110217
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Eshu Pty Ltd
Substance Name HOMOSALATE; OCTINOXATE; OCTISALATE
Strength Number 8; 3; 4
Strength Unit mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of moisturising sunscreen


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