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SHISEIDO
SHISEIDO - 52686-677-60 - (Octinoxate, Octocrylene, and Zinc oxide)
Drug Information of SHISEIDO
| Product NDC: | 52686-677 |
| Proprietary Name: | SHISEIDO |
| Non Proprietary Name: | Octinoxate, Octocrylene, and Zinc oxide |
| Active Ingredient(s): | 2.50047; 1.5309; 3.41901 g/51.03g; g/51.03g; g/51.03g & nbsp; Octinoxate, Octocrylene, and Zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SHISEIDO
| Product NDC: | 52686-677 |
| Labeler Name: | SHISEIDO AMERICA INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110201 |
Package Information of SHISEIDO
| Package NDC: | 52686-677-60 |
| Package Description: | 1 TUBE in 1 CARTON (52686-677-60) > 51.03 g in 1 TUBE |
NDC Information of SHISEIDO
| NDC Code | 52686-677-60 |
| Proprietary Name | SHISEIDO |
| Package Description | 1 TUBE in 1 CARTON (52686-677-60) > 51.03 g in 1 TUBE |
| Product NDC | 52686-677 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octocrylene, and Zinc oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SHISEIDO AMERICA INC. |
| Substance Name | OCTINOXATE; OCTOCRYLENE; ZINC OXIDE |
| Strength Number | 2.50047; 1.5309; 3.41901 |
| Strength Unit | g/51.03g; g/51.03g; g/51.03g |
| Pharmaceutical Classes |
