EASYDERM BAND

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: EASYDERM BAND
Generic name: PINE RESIN
Manufacturer: Lydia Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: f468decc-bc8d-f56c-e053-2a95a90ab43f
SPL ID: f468dee0-c460-9f28-e053-2a95a90a9834
Version: 1
Effective date: 2023-02-11
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:09:45

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 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		EASYDERM BAND	openfda.brand_name
generic name		PINE RESIN	openfda.generic_name
manufacturer name		Lydia Co., Ltd.	openfda.manufacturer_name
ndc	package	72988-0037-1	openfda.package_ndc
ndc	product	72988-0037	openfda.product_ndc
ndc11	package	72988003701	derived:openfda.package_ndc
spl id		f468dee0-c460-9f28-e053-2a95a90a9834	id
spl set id		f468decc-bc8d-f56c-e053-2a95a90ab43f	set_id
unii		QN24CZ7D5J	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

■ Check the expiration date. ■ If you experience allergic reactions or infection symptoms such as rash, fever, or itching while using this product, stop using it immediately and receive appropriate treatment according to the doctor's instructions.

Reported adverse events (FAERS/openFDA)#

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