NDC Labeler Sola Pharmaceuticals, Llc

Sola Pharmaceuticals, Llc labeler's code is 70512. The labeler has 18 products that have an assigned National Drug Code.

NDC	Proprietary Name	Non-Proprietary Name	Dosage Form	Route Name	Product Type	Status
70512-012	Lidaflex	Lidocaine	Patch	Topical	Human Otc Drug	ACTIVE
70512-013	Lenzapro Flex	Lidocaine/menthol	Patch	Topical	Human Otc Drug	ACTIVE
70512-014	Lidocaine 4% Patch	Lidocaine 4%	Patch	Topical	Human Otc Drug	ACTIVE
70512-015	Synoflex Patch	Synoflex Patch	Patch	Topical	Human Otc Drug	ACTIVE
70512-016	Capsimide	Capsaicin 0.025% Topical Patch	Patch	Topical	Human Otc Drug	ACTIVE
70512-017	Triceptin	Lidocaine / Menthol / Methyl Salicylate	Patch	Topical	Human Otc Drug	ACTIVE
70512-038	Diclofenac Sodium 1.5%	Diclofenac Sodium Topical	Solution	Topical	Human Prescription Drug	ACTIVE
70512-100	Clotrimazole Cream 1%	Clotrimazole Cream 1%	Cream	Topical	Human Otc Drug	ACTIVE
70512-101	Hydrocortisone Cream 1%	Hydrocortisone Cream 1%	Cream	Topical	Human Otc Drug	ACTIVE
70512-102	Triple Antibiotic	Triple Antibiotic	Ointment	Topical	Human Otc Drug	ACTIVE
70512-103	Zinc Oxide 20%	Zinc Oxide 20%	Ointment	Topical	Human Otc Drug	ACTIVE
70512-104	Neuracin Topical Gel	Neuracin Topical Analgesic Gel	Gel	Topical	Human Otc Drug	ACTIVE
70512-106	Diclofenac Sodium	Diclofenac Sodium 1%	Gel	Topical	Human Otc Drug	ACTIVE
70512-520	Olopatadine Hcl	Olopatadine Hcl	Solution/ Drops	Ophthalmic	Human Otc Drug	ACTIVE
70512-840	Cyanocobalamin	Cyanocobalamin	Injection	Intramuscular; Subcutaneous	Human Prescription Drug	ACTIVE
70512-851	Teriflunomide	Teriflunomide	Tablet, Coated	Oral	Human Prescription Drug	ACTIVE
70512-852	Dimethyl Fumarate	Dimethyl Fumarate	Capsule, Delayed Release	Oral	Human Prescription Drug	ACTIVE
70512-853	Dimethyl Fumarate	Dimethyl Fumarate	Capsule, Delayed Release	Oral	Human Prescription Drug	ACTIVE