| Product NDC: | 52686-280 |
| Proprietary Name: | SHISEIDO WHITE LUCENT BRIGHTENING PROTECTIVE W |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, and OCTOCRYLENE |
| Active Ingredient(s): | 1284; 3800; 1027 mg/51.35g; mg/51.35g; mg/51.35g & nbsp; AVOBENZONE, OCTINOXATE, and OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52686-280 |
| Labeler Name: | SHISEIDO AMERICA INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121101 |
| Package NDC: | 52686-280-50 |
| Package Description: | 1 JAR in 1 CARTON (52686-280-50) > 51.35 g in 1 JAR |
| NDC Code | 52686-280-50 |
| Proprietary Name | SHISEIDO WHITE LUCENT BRIGHTENING PROTECTIVE W |
| Package Description | 1 JAR in 1 CARTON (52686-280-50) > 51.35 g in 1 JAR |
| Product NDC | 52686-280 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTINOXATE, and OCTOCRYLENE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SHISEIDO AMERICA INC. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTOCRYLENE |
| Strength Number | 1284; 3800; 1027 |
| Strength Unit | mg/51.35g; mg/51.35g; mg/51.35g |
| Pharmaceutical Classes |