| Product NDC: | 64760-205 |
| Proprietary Name: | Glytone acne treatment |
| Non Proprietary Name: | salicylic acid |
| Active Ingredient(s): | 4.8 mL/240mL & nbsp; salicylic acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64760-205 |
| Labeler Name: | Glytone |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100101 |
| Package NDC: | 64760-205-01 |
| Package Description: | 240 BOTTLE, PLASTIC in 1 CARTON (64760-205-01) > 240 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 64760-205-01 |
| Proprietary Name | Glytone acne treatment |
| Package Description | 240 BOTTLE, PLASTIC in 1 CARTON (64760-205-01) > 240 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 64760-205 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | salicylic acid |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Glytone |
| Substance Name | SALICYLIC ACID |
| Strength Number | 4.8 |
| Strength Unit | mL/240mL |
| Pharmaceutical Classes |