Home
>
National Drug Code (NDC)
>
SHISEIDO WHITE LUCENT
SHISEIDO WHITE LUCENT - 52686-227-50 - (Ensulizole, Octinoxate, and Titanium Dioxide)
Drug Information of SHISEIDO WHITE LUCENT
| Product NDC: | 52686-227 |
| Proprietary Name: | SHISEIDO WHITE LUCENT |
| Non Proprietary Name: | Ensulizole, Octinoxate, and Titanium Dioxide |
| Active Ingredient(s): | 1.275; 3.774; .969 g/51g; g/51g; g/51g & nbsp; Ensulizole, Octinoxate, and Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SHISEIDO WHITE LUCENT
| Product NDC: | 52686-227 |
| Labeler Name: | SHISEIDO AMERICA INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100201 |
Package Information of SHISEIDO WHITE LUCENT
| Package NDC: | 52686-227-50 |
| Package Description: | 1 JAR in 1 CARTON (52686-227-50) > 51 g in 1 JAR |
NDC Information of SHISEIDO WHITE LUCENT
| NDC Code | 52686-227-50 |
| Proprietary Name | SHISEIDO WHITE LUCENT |
| Package Description | 1 JAR in 1 CARTON (52686-227-50) > 51 g in 1 JAR |
| Product NDC | 52686-227 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ensulizole, Octinoxate, and Titanium Dioxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SHISEIDO AMERICA INC. |
| Substance Name | ENSULIZOLE; OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 1.275; 3.774; .969 |
| Strength Unit | g/51g; g/51g; g/51g |
| Pharmaceutical Classes |
