| 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 |