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SHISEIDO SUNCARE EXTRA SMOOTH
SHISEIDO SUNCARE EXTRA SMOOTH - 52686-222-60 - (Octinoxate and Zinc Oxide)
Drug Information of SHISEIDO SUNCARE EXTRA SMOOTH
| Product NDC: | 52686-222 |
| Proprietary Name: | SHISEIDO SUNCARE EXTRA SMOOTH |
| Non Proprietary Name: | Octinoxate and Zinc Oxide |
| Active Ingredient(s): | 4.2; 5.5 g/57g; g/57g & nbsp; Octinoxate and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SHISEIDO SUNCARE EXTRA SMOOTH
| Product NDC: | 52686-222 |
| 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 SUNCARE EXTRA SMOOTH
| Package NDC: | 52686-222-60 |
| Package Description: | 1 TUBE in 1 CARTON (52686-222-60) > 57 g in 1 TUBE |
NDC Information of SHISEIDO SUNCARE EXTRA SMOOTH
| NDC Code | 52686-222-60 |
| Proprietary Name | SHISEIDO SUNCARE EXTRA SMOOTH |
| Package Description | 1 TUBE in 1 CARTON (52686-222-60) > 57 g in 1 TUBE |
| Product NDC | 52686-222 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Zinc Oxide |
| 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 | OCTINOXATE; ZINC OXIDE |
| Strength Number | 4.2; 5.5 |
| Strength Unit | g/57g; g/57g |
| Pharmaceutical Classes |
