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SHISEIDO ADVANCED HYDRO-LIQUID COMPACT (REFILL)
SHISEIDO ADVANCED HYDRO-LIQUID COMPACT (REFILL) - 52685-352-30 - (Titanium dioxide)
Drug Information of SHISEIDO ADVANCED HYDRO-LIQUID COMPACT (REFILL)
| Product NDC: | 52685-352 |
| Proprietary Name: | SHISEIDO ADVANCED HYDRO-LIQUID COMPACT (REFILL) |
| Non Proprietary Name: | Titanium dioxide |
| Active Ingredient(s): | .54 g/12g & nbsp; Titanium dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SHISEIDO ADVANCED HYDRO-LIQUID COMPACT (REFILL)
| Product NDC: | 52685-352 |
| Labeler Name: | SHISEIDO CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110801 |
Package Information of SHISEIDO ADVANCED HYDRO-LIQUID COMPACT (REFILL)
| Package NDC: | 52685-352-30 |
| Package Description: | 1 TRAY in 1 CARTON (52685-352-30) > 12 g in 1 TRAY |
NDC Information of SHISEIDO ADVANCED HYDRO-LIQUID COMPACT (REFILL)
| NDC Code | 52685-352-30 |
| Proprietary Name | SHISEIDO ADVANCED HYDRO-LIQUID COMPACT (REFILL) |
| Package Description | 1 TRAY in 1 CARTON (52685-352-30) > 12 g in 1 TRAY |
| Product NDC | 52685-352 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium dioxide |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SHISEIDO CO., LTD. |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | .54 |
| Strength Unit | g/12g |
| Pharmaceutical Classes |
