| 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 |