Bactine Max Bandage

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Bactine Max Bandage
Generic name: LIDOCAINE
Manufacturer: WellSpring Pharmaceutical Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 465dc46e-6435-4569-9516-f648d0fe0f09
SPL ID: ce780255-5bba-4e68-ad28-279f0ca6b187
Version: 3
Effective date: 2023-12-21
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:04:29

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Bactine Max Bandage	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		WellSpring Pharmaceutical Corporation	openfda.manufacturer_name
ndc	package	65197-830-00	openfda.package_ndc
ndc	product	65197-830	openfda.product_ndc
ndc11	package	65197083000	derived:openfda.package_ndc
spl id		ce780255-5bba-4e68-ad28-279f0ca6b187	id
spl set id		465dc46e-6435-4569-9516-f648d0fe0f09	set_id
unii		V13007Z41A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use If you are allergic to any of the ingredients in or near the eyes over large areas of the body longer than 1 week unless directed by a doctor Ask a doctor before use if you have deep or puncture wounds deep cuts animal bites serious burns When using this product do not apply over raw surfaces or blistered areas Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days, or clear up and occur again within a few days Keep out of reach of children If swallowed, call a poison control center or get medical help right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.