Dr.Johnes Liquid Skin Wart Corn Remover

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: Dr.Johnes Liquid Skin Wart Corn Remover
Generic name: SALICYLIC ACID
Manufacturer: Dr.Johnes LLC
Product type: HUMAN OTC DRUG
SPL set ID: f9efe02a-abc9-4a2f-afb0-9d358fc35c91
SPL ID: faae55c8-da42-4ee6-8717-6c177e7271eb
Version: 4
Effective date: 2026-05-22
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:48:42

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M028	openfda.application_number
brand name		Dr.Johnes Liquid Skin Wart Corn Remover	openfda.brand_name
generic name		SALICYLIC ACID	openfda.generic_name
manufacturer name		Dr.Johnes LLC	openfda.manufacturer_name
ndc	package	85818-004-01	openfda.package_ndc
ndc	package	85818-004-05	openfda.package_ndc
ndc	package	85818-004-06	openfda.package_ndc
ndc	package	85818-004-03	openfda.package_ndc
ndc	package	85818-004-04	openfda.package_ndc
ndc	package	85818-004-02	openfda.package_ndc
ndc	product	85818-004	openfda.product_ndc
ndc11	package	85818000406	derived:openfda.package_ndc
ndc11	package	85818000405	derived:openfda.package_ndc
ndc11	package	85818000404	derived:openfda.package_ndc
ndc11	package	85818000402	derived:openfda.package_ndc
ndc11	package	85818000401	derived:openfda.package_ndc
ndc11	package	85818000403	derived:openfda.package_ndc
rxcui		312881	openfda.rxcui
spl id		faae55c8-da42-4ee6-8717-6c177e7271eb	id
spl set id		f9efe02a-abc9-4a2f-afb0-9d358fc35c91	set_id
unii		O414PZ4LPZ	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

For external use only Do not use: Face Genital warts Moles Birthmarks Open wounds Irritated skin Infected skin Mucous membranes Ask a doctor before use if you have diabetes or poor blood circulation. Stop use and ask a doctor if discomfort, burning, redness or irritation occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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