Nurture ANTISEPTIC 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: Nurture ANTISEPTIC WIPES
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Devon Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: ff2c761f-1a82-467b-9a5f-a2cdbd2be935
SPL ID: e8d9314b-5e84-4f21-b2bd-2b78903d0193
Version: 4
Effective date: 2025-04-02
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:13

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Nurture ANTISEPTIC WIPES	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Devon Products, LLC	openfda.manufacturer_name
ndc	package	81072-001-12	openfda.package_ndc
ndc	package	81072-001-11	openfda.package_ndc
ndc	package	81072-001-13	openfda.package_ndc
ndc	package	81072-001-03	openfda.package_ndc
ndc	package	81072-001-01	openfda.package_ndc
ndc	package	81072-001-02	openfda.package_ndc
ndc	package	81072-001-04	openfda.package_ndc
ndc	package	81072-001-14	openfda.package_ndc
ndc	product	81072-001	openfda.product_ndc
ndc11	package	81072000112	derived:openfda.package_ndc
ndc11	package	81072000103	derived:openfda.package_ndc
ndc11	package	81072000102	derived:openfda.package_ndc
ndc11	package	81072000114	derived:openfda.package_ndc
ndc11	package	81072000111	derived:openfda.package_ndc
ndc11	package	81072000113	derived:openfda.package_ndc
ndc11	package	81072000101	derived:openfda.package_ndc
ndc11	package	81072000104	derived:openfda.package_ndc
rxcui		1038558	openfda.rxcui
spl id		e8d9314b-5e84-4f21-b2bd-2b78903d0193	id
spl set id		ff2c761f-1a82-467b-9a5f-a2cdbd2be935	set_id
unii		F5UM2KM3W7	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 Do not use • on children less than 2 months of age • on open skin wounds • if you are allergic to any of the ingredients When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water Stop use and ask a doctor if • irritation and redness develop • condition persists for more than 72 hours 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.