Product NDC: | 62874-005 |
Proprietary Name: | VITAMIN E DAY |
Non Proprietary Name: | OCTISALATE, AVOBENZONE |
Active Ingredient(s): | 3; 5 mL/100mL; mL/100mL & nbsp; OCTISALATE, AVOBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62874-005 |
Labeler Name: | JO MALONE LTD |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110501 |
Package NDC: | 62874-005-01 |
Package Description: | 50 mL in 1 JAR (62874-005-01) |
NDC Code | 62874-005-01 |
Proprietary Name | VITAMIN E DAY |
Package Description | 50 mL in 1 JAR (62874-005-01) |
Product NDC | 62874-005 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTISALATE, AVOBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110501 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | JO MALONE LTD |
Substance Name | AVOBENZONE; OCTISALATE |
Strength Number | 3; 5 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |