EasyStick

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: EasyStick
Generic name: SODIUM CHLORITE
Manufacturer: Pure O2
Product type: HUMAN OTC DRUG
SPL set ID: a39b9ce6-a074-4165-e053-2995a90a277a
SPL ID: 0a4eb0be-cd46-6702-e063-6294a90ab9a3
Version: 3
Effective date: 2023-11-16
Source export date: 2026-10-30
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:37:55

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 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		EasyStick	openfda.brand_name
generic name		SODIUM CHLORITE	openfda.generic_name
manufacturer name		Pure O2	openfda.manufacturer_name
ndc	package	75124-0004-1	openfda.package_ndc
ndc	product	75124-0004	openfda.product_ndc
ndc11	package	75124000401	derived:openfda.package_ndc
spl id		0a4eb0be-cd46-6702-e063-6294a90ab9a3	id
spl set id		a39b9ce6-a074-4165-e053-2995a90a277a	set_id
unii		G538EBV4VF	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

■ For external use only. ■ Do not use in eyes. ■ lf swallowed, get medical help promptly. ■ Stop use, ask doctor lf irritation occurs. ■ Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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