Product NDC: | 49825-114 |
Proprietary Name: | Bioelements |
Non Proprietary Name: | Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide, Zinc Oxide |
Active Ingredient(s): | 7.5; 5; 3; .01; .01 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide, Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49825-114 |
Labeler Name: | Bioelements Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090101 |
Package NDC: | 49825-114-02 |
Package Description: | 1 BOTTLE in 1 BOX (49825-114-02) > 177 mL in 1 BOTTLE (49825-114-01) |
NDC Code | 49825-114-02 |
Proprietary Name | Bioelements |
Package Description | 1 BOTTLE in 1 BOX (49825-114-02) > 177 mL in 1 BOTTLE (49825-114-01) |
Product NDC | 49825-114 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide, Zinc Oxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20090101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Bioelements Inc. |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 7.5; 5; 3; .01; .01 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |