XtraCare Wet 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: XtraCare Wet Wipes
Generic name: BENZETHONIUM CHLORIDE
Manufacturer: Rejoice International
Product type: HUMAN OTC DRUG
SPL set ID: 3741acc3-c590-4bf1-8c83-4f812e2c7adc
SPL ID: 2decd513-1fc5-1793-e063-6294a90a18bf
Version: 3
Effective date: 2025-02-12
Source export date: 2026-10-27
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/2026-10-27/6f51a1483736359ffd78ed7be27289bc51f2a8463b934465bee40efbdef4dfd7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 21:07:11

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		XtraCare Wet Wipes	openfda.brand_name
generic name		BENZETHONIUM CHLORIDE	openfda.generic_name
manufacturer name		Rejoice International	openfda.manufacturer_name
ndc	package	57337-062-01	openfda.package_ndc
ndc	product	57337-062	openfda.product_ndc
ndc11	package	57337006201	derived:openfda.package_ndc
rxcui		1043348	openfda.rxcui
spl id		2decd513-1fc5-1793-e063-6294a90a18bf	id
spl set id		3741acc3-c590-4bf1-8c83-4f812e2c7adc	set_id
unii		PH41D05744	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 if you are allergic to any of the ingredients. When using this product do not get into eyes. If eye contact occurs, rinse thoroughly with water. Stop use and ask a doctor if irritation and redness develops, and continues for more than 72 hours.

Reported adverse events (FAERS/openFDA)#

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