eha

Generic: lidocaine hydrochloride

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name eha
Generic Name lidocaine hydrochloride
Labeler asclemed usa, inc.
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

lidocaine hydrochloride 4 g/mL

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-351
Product ID 76420-351_7d77ecf6-5731-d43e-e053-2991aa0af0db
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2016-06-07

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 76420351
Hyphenated Format 76420-351

Supplemental Identifiers

UPC
0376420351306
UNII
V13007Z41A

Packaging Origin

Original Packager
true

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 eha (source: ndc)
Generic Name lidocaine hydrochloride (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 4 g/mL
source: ndc
Packaging
  • 88 mL in 1 BOTTLE (76420-351-30)
source: ndc

Packages (1)

Ingredients (1)

lidocaine hydrochloride (4 g/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "7d77ecf6-5731-d43e-e053-2991aa0af0db", "openfda": {"upc": ["0376420351306"], "unii": ["V13007Z41A"], "spl_set_id": ["09835640-55c3-4bfa-9ad3-15d37f06e871"], "manufacturer_name": ["Asclemed USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "88 mL in 1 BOTTLE (76420-351-30)", "package_ndc": "76420-351-30", "marketing_start_date": "20160607"}], "brand_name": "Eha", "product_id": "76420-351_7d77ecf6-5731-d43e-e053-2991aa0af0db", "dosage_form": "LOTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "76420-351", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eha", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "4 g/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20160607", "listing_expiration_date": "20261231"}