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CICLOFERON
CICLOFERON - 75940-122-02 - (benzalkonium chloride and lidocaine hydrochloride)
Drug Information of CICLOFERON
| Product NDC: | 75940-122 |
| Proprietary Name: | CICLOFERON |
| Non Proprietary Name: | benzalkonium chloride and lidocaine hydrochloride |
| Active Ingredient(s): | 20; 1.3 mg/g; mg/g & nbsp; benzalkonium chloride and lidocaine hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CICLOFERON
| Product NDC: | 75940-122 |
| Labeler Name: | MarcasUSA LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110801 |
Package Information of CICLOFERON
| Package NDC: | 75940-122-02 |
| Package Description: | 1 TUBE in 1 CARTON (75940-122-02) > 2 g in 1 TUBE |
NDC Information of CICLOFERON
| NDC Code | 75940-122-02 |
| Proprietary Name | CICLOFERON |
| Package Description | 1 TUBE in 1 CARTON (75940-122-02) > 2 g in 1 TUBE |
| Product NDC | 75940-122 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzalkonium chloride and lidocaine hydrochloride |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MarcasUSA LLC |
| Substance Name | BENZALKONIUM CHLORIDE; LIDOCAINE HYDROCHLORIDE |
| Strength Number | 20; 1.3 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
