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SHISEIDO WHITE LUCENT
SHISEIDO WHITE LUCENT - 52686-228-10 - (Octinoxate and Octocrylene)
Drug Information of SHISEIDO WHITE LUCENT
| Product NDC: | 52686-228 |
| Proprietary Name: | SHISEIDO WHITE LUCENT |
| Non Proprietary Name: | Octinoxate and Octocrylene |
| Active Ingredient(s): | 3.479; 3.55 g/71g; g/71g & nbsp; Octinoxate and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SHISEIDO WHITE LUCENT
| Product NDC: | 52686-228 |
| 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 WHITE LUCENT
| Package NDC: | 52686-228-10 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (52686-228-10) > 71 g in 1 BOTTLE, PUMP |
NDC Information of SHISEIDO WHITE LUCENT
| NDC Code | 52686-228-10 |
| Proprietary Name | SHISEIDO WHITE LUCENT |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (52686-228-10) > 71 g in 1 BOTTLE, PUMP |
| Product NDC | 52686-228 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Octocrylene |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SHISEIDO AMERICA INC. |
| Substance Name | OCTINOXATE; OCTOCRYLENE |
| Strength Number | 3.479; 3.55 |
| Strength Unit | g/71g; g/71g |
| Pharmaceutical Classes |
