Product NDC: | 52686-281 |
Proprietary Name: | SHISEIDO WHITE LUCENT BRIGHTENING PROTECTIVE W |
Non Proprietary Name: | AVOBENZONE, OCTINOXATE, and OCTOCRYLENE |
Active Ingredient(s): | 1915; 5667; 1532 mg/76.58g; mg/76.58g; mg/76.58g & nbsp; AVOBENZONE, OCTINOXATE, and OCTOCRYLENE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | EMULSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52686-281 |
Labeler Name: | SHISEIDO AMERICA INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121101 |
Package NDC: | 52686-281-11 |
Package Description: | 1 BOTTLE in 1 CARTON (52686-281-11) > 7.15 g in 1 BOTTLE |
NDC Code | 52686-281-11 |
Proprietary Name | SHISEIDO WHITE LUCENT BRIGHTENING PROTECTIVE W |
Package Description | 1 BOTTLE in 1 CARTON (52686-281-11) > 7.15 g in 1 BOTTLE |
Product NDC | 52686-281 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, OCTINOXATE, and OCTOCRYLENE |
Dosage Form Name | EMULSION |
Route Name | TOPICAL |
Start Marketing Date | 20121101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | SHISEIDO AMERICA INC. |
Substance Name | AVOBENZONE; OCTINOXATE; OCTOCRYLENE |
Strength Number | 1915; 5667; 1532 |
Strength Unit | mg/76.58g; mg/76.58g; mg/76.58g |
Pharmaceutical Classes |