Sting Relief 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: Sting Relief Wipes
Generic name: STING RELIEF WIPES
Manufacturer: ProStat First Aid LLC
Product type: HUMAN OTC DRUG
SPL set ID: 0e20252a-5ecb-2526-e063-6294a90a8cde
SPL ID: 4601810d-1e03-140b-e063-6294a90a8ff5
Version: 3
Effective date: 2025-12-15
Source export date: 2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:48:04

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Sting Relief Wipes	openfda.brand_name
generic name		STING RELIEF WIPES	openfda.generic_name
manufacturer name		ProStat First Aid LLC	openfda.manufacturer_name
ndc	package	58228-2204-1	openfda.package_ndc
ndc	product	58228-2204	openfda.product_ndc
ndc11	package	58228220401	derived:openfda.package_ndc
rxcui		895749	openfda.rxcui
spl id		4601810d-1e03-140b-e063-6294a90a8ff5	id
spl set id		0e20252a-5ecb-2526-e063-6294a90a8cde	set_id
unii		U3RSY48JW5	openfda.unii
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. When using • Avoid contact with eyes; if this occurs, rinse thoroughtly with water Do not use • With electrocautery procedures Stop use if • Irritation and redness develop • Condition worsens or symptoms persist for more than 7 days, or clear up and occur again within a few day; discontinue use and consult a doctor Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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