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SHISEIDO WHITE LUCENT
SHISEIDO WHITE LUCENT - 52686-251-60 - (OCTINOXATE and TITANIUM DIOXIDE)
Drug Information of SHISEIDO WHITE LUCENT
| Product NDC: | 52686-251 |
| Proprietary Name: | SHISEIDO WHITE LUCENT |
| Non Proprietary Name: | OCTINOXATE and TITANIUM DIOXIDE |
| Active Ingredient(s): | .9396; 2.7216 g/32.4g; g/32.4g & nbsp; OCTINOXATE and TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SHISEIDO WHITE LUCENT
| Product NDC: | 52686-251 |
| 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 WHITE LUCENT
| Package NDC: | 52686-251-60 |
| Package Description: | 1 TUBE in 1 CARTON (52686-251-60) > 32.4 g in 1 TUBE |
NDC Information of SHISEIDO WHITE LUCENT
| NDC Code | 52686-251-60 |
| Proprietary Name | SHISEIDO WHITE LUCENT |
| Package Description | 1 TUBE in 1 CARTON (52686-251-60) > 32.4 g in 1 TUBE |
| Product NDC | 52686-251 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and TITANIUM DIOXIDE |
| Dosage Form Name | PASTE |
| Route Name | TOPICAL |
| Start Marketing Date | 20110201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SHISEIDO AMERICA INC. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | .9396; 2.7216 |
| Strength Unit | g/32.4g; g/32.4g |
| Pharmaceutical Classes |
