NEXXGEN 50% RUBBING ALCOHOL

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 50% RUBBING ALCOHOL
Generic name: ISOPROPYL ALCOHOL
Manufacturer: A & A Nexxgen LLC
Product type: HUMAN OTC DRUG
SPL set ID: d48232ab-ab55-488a-9cc1-77c8d0ba992e
SPL ID: 6574f32f-35e2-4b35-9e67-abe99f47a352
Version: 3
Effective date: 2026-01-16
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:47

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 50% RUBBING ALCOHOL	openfda.brand_name
generic name		ISOPROPYL ALCOHOL	openfda.generic_name
manufacturer name		A & A Nexxgen LLC	openfda.manufacturer_name
ndc	package	83629-019-32	openfda.package_ndc
ndc	package	83629-019-16	openfda.package_ndc
ndc	package	83629-019-12	openfda.package_ndc
ndc	product	83629-019	openfda.product_ndc
ndc11	package	83629001916	derived:openfda.package_ndc
ndc11	package	83629001912	derived:openfda.package_ndc
ndc11	package	83629001932	derived:openfda.package_ndc
rxcui		616456	openfda.rxcui
spl id		6574f32f-35e2-4b35-9e67-abe99f47a352	id
spl set id		d48232ab-ab55-488a-9cc1-77c8d0ba992e	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.