Pharma care IPA Wipes

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: Pharma care IPA Wipes
Generic name: ISOPROPYL ALCOHOL
Manufacturer: Enviro Specialty Chemicals Inc
Product type: HUMAN OTC DRUG
SPL set ID: 26ce919a-1765-4b44-9114-24ea7383a987
SPL ID: 026535fc-4e39-4b5b-9937-49f584c4b205
Version: 4
Effective date: 2026-07-24
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 05:15:25

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 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Pharma care IPA Wipes	openfda.brand_name
generic name		ISOPROPYL ALCOHOL	openfda.generic_name
manufacturer name		Enviro Specialty Chemicals Inc	openfda.manufacturer_name
ndc	package	71884-013-02	openfda.package_ndc
ndc	package	71884-013-50	openfda.package_ndc
ndc	package	71884-013-20	openfda.package_ndc
ndc	package	71884-013-82	openfda.package_ndc
ndc	package	71884-013-80	openfda.package_ndc
ndc	package	71884-013-81	openfda.package_ndc
ndc	package	71884-013-88	openfda.package_ndc
ndc	package	71884-013-04	openfda.package_ndc
ndc	package	71884-013-03	openfda.package_ndc
ndc	package	71884-013-01	openfda.package_ndc
ndc	product	71884-013	openfda.product_ndc
ndc11	package	71884001382	derived:openfda.package_ndc
ndc11	package	71884001301	derived:openfda.package_ndc
ndc11	package	71884001303	derived:openfda.package_ndc
ndc11	package	71884001320	derived:openfda.package_ndc
ndc11	package	71884001304	derived:openfda.package_ndc
ndc11	package	71884001381	derived:openfda.package_ndc
ndc11	package	71884001388	derived:openfda.package_ndc
ndc11	package	71884001302	derived:openfda.package_ndc
ndc11	package	71884001380	derived:openfda.package_ndc
ndc11	package	71884001350	derived:openfda.package_ndc
rxcui		797544	openfda.rxcui
spl id		026535fc-4e39-4b5b-9937-49f584c4b205	id
spl set id		26ce919a-1765-4b44-9114-24ea7383a987	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: FLAMMABLE. Keep away from fire, electrical & spark For external use only. Do not use In ears, eyes or mouth. • Avoid contact with the eyes. In case of contact, flush eyes with water • Stop use and ask a doctor if redness or irritation develop and persist • If swallowed contact a poison center • Do not store above 110°F(43°C) • Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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