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