Product NDC: | 63014-1600 |
Proprietary Name: | SHISEIDO |
Non Proprietary Name: | Avobenzone and Octinoxate |
Active Ingredient(s): | 3.3; 9.768 g/132g; g/132g & nbsp; Avobenzone and Octinoxate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63014-1600 |
Labeler Name: | SHISEIDO INTERNATIONAL FRANCE |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20040803 |
Package NDC: | 63014-1600-1 |
Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (63014-1600-1) > 132 g in 1 BOTTLE, SPRAY |
NDC Code | 63014-1600-1 |
Proprietary Name | SHISEIDO |
Package Description | 1 BOTTLE, SPRAY in 1 CARTON (63014-1600-1) > 132 g in 1 BOTTLE, SPRAY |
Product NDC | 63014-1600 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone and Octinoxate |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20040803 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | SHISEIDO INTERNATIONAL FRANCE |
Substance Name | AVOBENZONE; OCTINOXATE |
Strength Number | 3.3; 9.768 |
Strength Unit | g/132g; g/132g |
Pharmaceutical Classes |