Product NDC: | 52554-3001 |
Proprietary Name: | Laser Block 100 |
Non Proprietary Name: | OCTINOXATE |
Active Ingredient(s): | .02; .005; .03; .07; .02; .05 mL/mL; mL/mL; mL/mL; mL/mL; mL/mL; mL/mL & nbsp; OCTINOXATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52554-3001 |
Labeler Name: | Universal Cosmetic Co., Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100804 |
Package NDC: | 52554-3001-1 |
Package Description: | 50 mL in 1 TUBE (52554-3001-1) |
NDC Code | 52554-3001-1 |
Proprietary Name | Laser Block 100 |
Package Description | 50 mL in 1 TUBE (52554-3001-1) |
Product NDC | 52554-3001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100804 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Universal Cosmetic Co., Ltd |
Substance Name | AMILOXATE; AVOBENZONE; ENZACAMENE; OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | .02; .005; .03; .07; .02; .05 |
Strength Unit | mL/mL; mL/mL; mL/mL; mL/mL; mL/mL; mL/mL |
Pharmaceutical Classes |