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Bioelements, Inc. - 49825-117-02 - (Homosalate, Octinoxate, Octisalate, Oxybenzone)

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Drug Information of Bioelements, Inc.

Product NDC: 49825-117
Proprietary Name: Bioelements, Inc.
Non Proprietary Name: Homosalate, Octinoxate, Octisalate, Oxybenzone
Active Ingredient(s): 10; 7.5; 5; 6    mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   Homosalate, Octinoxate, Octisalate, Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Bioelements, Inc.

Product NDC: 49825-117
Labeler Name: Bioelements, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100101

Package Information of Bioelements, Inc.

Package NDC: 49825-117-02
Package Description: 1 JAR in 1 BOX (49825-117-02) > 73 mL in 1 JAR (49825-117-01)

NDC Information of Bioelements, Inc.

NDC Code 49825-117-02
Proprietary Name Bioelements, Inc.
Package Description 1 JAR in 1 BOX (49825-117-02) > 73 mL in 1 JAR (49825-117-01)
Product NDC 49825-117
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Homosalate, Octinoxate, Octisalate, Oxybenzone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Bioelements, Inc.
Substance Name HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 10; 7.5; 5; 6
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Bioelements, Inc.


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