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SHISEIDO SUNCARE ULTIMATE
SHISEIDO SUNCARE ULTIMATE - 52686-226-10 - (Ensulizole, Octinoxate, and Zinc Oxide)
Drug Information of SHISEIDO SUNCARE ULTIMATE
| Product NDC: | 52686-226 |
| Proprietary Name: | SHISEIDO SUNCARE ULTIMATE |
| Non Proprietary Name: | Ensulizole, Octinoxate, and Zinc Oxide |
| Active Ingredient(s): | 1.88; 6.956; 15.322 g/94g; g/94g; g/94g & nbsp; Ensulizole, Octinoxate, and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SHISEIDO SUNCARE ULTIMATE
| Product NDC: | 52686-226 |
| 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 ULTIMATE
| Package NDC: | 52686-226-10 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (52686-226-10) > 94 g in 1 BOTTLE, PLASTIC |
NDC Information of SHISEIDO SUNCARE ULTIMATE
| NDC Code | 52686-226-10 |
| Proprietary Name | SHISEIDO SUNCARE ULTIMATE |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (52686-226-10) > 94 g in 1 BOTTLE, PLASTIC |
| Product NDC | 52686-226 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ensulizole, Octinoxate, and Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SHISEIDO AMERICA INC. |
| Substance Name | ENSULIZOLE; OCTINOXATE; ZINC OXIDE |
| Strength Number | 1.88; 6.956; 15.322 |
| Strength Unit | g/94g; g/94g; g/94g |
| Pharmaceutical Classes |
