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SHISEIDO
SHISEIDO - 52686-231-10 - (Octinoxate and Octocrylene)
Drug Information of SHISEIDO
| Product NDC: | 52686-231 |
| Proprietary Name: | SHISEIDO |
| Non Proprietary Name: | Octinoxate and Octocrylene |
| Active Ingredient(s): | 3.81465; 3.8925 g/77.85g; g/77.85g & nbsp; Octinoxate and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SHISEIDO
| Product NDC: | 52686-231 |
| 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: | 52686-231-10 |
| Package Description: | 1 BOTTLE in 1 CARTON (52686-231-10) > 77.85 g in 1 BOTTLE |
NDC Information of SHISEIDO
| NDC Code | 52686-231-10 |
| Proprietary Name | SHISEIDO |
| Package Description | 1 BOTTLE in 1 CARTON (52686-231-10) > 77.85 g in 1 BOTTLE |
| Product NDC | 52686-231 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Octocrylene |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SHISEIDO AMERICA INC. |
| Substance Name | OCTINOXATE; OCTOCRYLENE |
| Strength Number | 3.81465; 3.8925 |
| Strength Unit | g/77.85g; g/77.85g |
| Pharmaceutical Classes |
