Label: ANTISEPTIC- alcohol, lidocaine hydrochloride liquid
-
NDC Code(s):
61010-5200-1,
61010-5200-2,
61010-5200-3,
61010-5200-4, view more61010-5200-5, 61010-5200-6, 61010-5200-7
- Packager: Safetec of America, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 7, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Uses
- Warnings
- Directions
- PRINCIPAL DISPLAY PANEL – mini pouch label
- PRINCIPAL DISPLAY PANEL – 150 count box
- PRINCIPAL DISPLAY PANEL – 2 fl. oz. bottle
- Principal Display Panel – 25 Count Box Label
-
INGREDIENTS AND APPEARANCE
ANTISEPTIC
alcohol, lidocaine hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61010-5200 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 500 mg in 1 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg in 1 g Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61010-5200-1 56 g in 1 BOTTLE; Type 0: Not a Combination Product 09/30/2011 2 NDC:61010-5200-4 150 in 1 BOX 09/30/2011 2 NDC:61010-5200-3 0.8 g in 1 PACKET; Type 0: Not a Combination Product 3 NDC:61010-5200-5 10 in 1 BOX 09/30/2011 3 NDC:61010-5200-3 0.8 g in 1 PACKET; Type 0: Not a Combination Product 4 NDC:61010-5200-2 100 in 1 BOX 09/30/2011 4 1.8 g in 1 PACKET; Type 0: Not a Combination Product 5 NDC:61010-5200-6 20 in 1 BOX 09/30/2011 5 1.8 g in 1 PACKET; Type 0: Not a Combination Product 6 NDC:61010-5200-7 25 in 1 BOX 09/30/2011 6 1.8 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 09/30/2011 Labeler - Safetec of America, Inc. (874965262) Establishment Name Address ID/FEI Business Operations Safetec of America, Inc. 874965262 manufacture(61010-5200)