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DOUBLE MATTE
DOUBLE MATTE - 11559-732-01 - (OCTINOXATE)
Drug Information of DOUBLE MATTE
| Product NDC: | 11559-732 |
| Proprietary Name: | DOUBLE MATTE |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 2.2 mL/100mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOUBLE MATTE
| Product NDC: | 11559-732 |
| Labeler Name: | Estee Lauder Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19980101 |
Package Information of DOUBLE MATTE
| Package NDC: | 11559-732-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (11559-732-01) > 30 mL in 1 BOTTLE |
NDC Information of DOUBLE MATTE
| NDC Code | 11559-732-01 |
| Proprietary Name | DOUBLE MATTE |
| Package Description | 1 BOTTLE in 1 CARTON (11559-732-01) > 30 mL in 1 BOTTLE |
| Product NDC | 11559-732 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 19980101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Estee Lauder Inc. |
| Substance Name | OCTINOXATE |
| Strength Number | 2.2 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
