North Woods Derma Gel Clear

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: North Woods Derma Gel Clear
Generic name: ALCOHOL
Manufacturer: Superior Chemical Corporation
Product type: HUMAN OTC DRUG
SPL set ID: abbd099a-8d89-80a0-e053-2a95a90a24fc
SPL ID: 40a72db6-d505-3e66-e063-6294a90a6566
Version: 4
Effective date: 2025-10-08
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:38:01

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		North Woods Derma Gel Clear	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Superior Chemical Corporation	openfda.manufacturer_name
ndc	package	53125-801-29	openfda.package_ndc
ndc	package	53125-801-04	openfda.package_ndc
ndc	package	53125-801-57	openfda.package_ndc
ndc	package	53125-801-09	openfda.package_ndc
ndc	product	53125-801	openfda.product_ndc
ndc11	package	53125080157	derived:openfda.package_ndc
ndc11	package	53125080104	derived:openfda.package_ndc
ndc11	package	53125080109	derived:openfda.package_ndc
ndc11	package	53125080129	derived:openfda.package_ndc
rxcui		581662	openfda.rxcui
spl id		40a72db6-d505-3e66-e063-6294a90a6566	id
spl set id		abbd099a-8d89-80a0-e053-2a95a90a24fc	set_id
unii		3K9958V90M	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 Warnings • For external use only. • Avoid contact with eyes. If contact occurs, rinse thoroughly with water. • FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition. • Discontinue use if irritation or redness develops. • If irritation persists for more than 72 hours, consult a physician. • 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.