NEXXGEN 91% RUBBING ALCOHOL with Wintergreen

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: NEXXGEN 91% RUBBING ALCOHOL with Wintergreen
Generic name: ISOPROPYL ALCOHOL
Manufacturer: A & A Nexxgen LLC
Product type: HUMAN OTC DRUG
SPL set ID: 12b8c85a-da0c-47a1-9531-c9f2858c4f31
SPL ID: 8c0dd90b-81f4-474b-a3f3-3532dc5d1652
Version: 3
Effective date: 2024-12-09
Source export date: 2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:55:49

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		NEXXGEN 91% RUBBING ALCOHOL with Wintergreen	openfda.brand_name
generic name		ISOPROPYL ALCOHOL	openfda.generic_name
manufacturer name		A & A Nexxgen LLC	openfda.manufacturer_name
ndc	package	83629-018-32	openfda.package_ndc
ndc	package	83629-018-16	openfda.package_ndc
ndc	package	83629-018-12	openfda.package_ndc
ndc	product	83629-018	openfda.product_ndc
ndc11	package	83629001816	derived:openfda.package_ndc
ndc11	package	83629001832	derived:openfda.package_ndc
ndc11	package	83629001812	derived:openfda.package_ndc
rxcui		582901	openfda.rxcui
spl id		8c0dd90b-81f4-474b-a3f3-3532dc5d1652	id
spl set id		12b8c85a-da0c-47a1-9531-c9f2858c4f31	set_id
unii		ND2M416302	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; flammable, keep away from fire or flame, heat, spark, electrical Ask a doctor before use if you have • deep punctured wounds, animal bites or serious burns When using this product • do not get into eyes • do not apply over large areas of the body • do not use longer than one week unless directed by a doctor Stop using this product if • condition persists or gets worse Keep this and all drugs out of the reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison control center (1‑800‑222‑1222) immediately.

Reported adverse events (FAERS/openFDA)#

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