antibacterial lidocaine wound gel

Generic: benzalkonium chloride, lidocaine hydrochloride

Labeler: aso llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name antibacterial lidocaine wound gel
Generic Name benzalkonium chloride, lidocaine hydrochloride
Labeler aso llc
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

benzalkonium chloride .13 g/100mL, lidocaine hydrochloride 2 g/100mL

Manufacturer
ASO LLC

Identifiers & Regulatory

Product NDC 51142-652
Product ID 51142-652_262f971a-aa6f-8cd4-e063-6394a90a40b0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2019-10-28

Pharmacologic Class

Classes
amide local anesthetic [epc] amides [cs] antiarrhythmic [epc] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51142652
Hyphenated Format 51142-652

Supplemental Identifiers

RxCUI
1431682
UNII
F5UM2KM3W7 V13007Z41A

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name antibacterial lidocaine wound gel (source: ndc)
Generic Name benzalkonium chloride, lidocaine hydrochloride (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .13 g/100mL
  • 2 g/100mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51142-652-14) / 14 mL in 1 TUBE
  • 1 TUBE in 1 CARTON (51142-652-28) / 28 mL in 1 TUBE
source: ndc

Packages (2)

51142-652-14 1 TUBE in 1 CARTON (51142-652-14) / 14 mL in 1 TUBE 51142-652-28 1 TUBE in 1 CARTON (51142-652-28) / 28 mL in 1 TUBE

Ingredients (2)

benzalkonium chloride (.13 g/100mL) lidocaine hydrochloride (2 g/100mL)

Linked Drug Pages (1)

Antibacterial Lidocaine Wound Gel ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "262f971a-aa6f-8cd4-e063-6394a90a40b0", "openfda": {"unii": ["F5UM2KM3W7", "V13007Z41A"], "rxcui": ["1431682"], "spl_set_id": ["cb9505b7-222d-3a24-e053-2a95a90a0b64"], "manufacturer_name": ["ASO LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51142-652-14)  / 14 mL in 1 TUBE", "package_ndc": "51142-652-14", "marketing_start_date": "20191028"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51142-652-28)  / 28 mL in 1 TUBE", "package_ndc": "51142-652-28", "marketing_start_date": "20191028"}], "brand_name": "Antibacterial Lidocaine Wound Gel", "product_id": "51142-652_262f971a-aa6f-8cd4-e063-6394a90a40b0", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "51142-652", "generic_name": "benzalkonium chloride, lidocaine hydrochloride", "labeler_name": "ASO LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antibacterial Lidocaine Wound Gel", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".13 g/100mL"}, {"name": "LIDOCAINE HYDROCHLORIDE", "strength": "2 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191028", "listing_expiration_date": "20261231"}