SannyTize Hand Sanitizer

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: SannyTize Hand Sanitizer
Generic name: HAND SANITIZER
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 968713a5-64d3-86fc-e053-2995a90a088a
SPL ID: 0fb7cb81-bb4b-f99f-e063-6294a90a336b
Version: 4
Effective date: 2024-01-24
Source export date: 2026-10-12
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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:45:32

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 2 · 43 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		SannyTize Hand Sanitizer	openfda.brand_name
generic name		HAND SANITIZER	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-010-15	openfda.package_ndc
ndc	package	67777-010-02	openfda.package_ndc
ndc	package	67777-010-20	openfda.package_ndc
ndc	package	67777-010-12	openfda.package_ndc
ndc	package	67777-010-18	openfda.package_ndc
ndc	package	67777-010-19	openfda.package_ndc
ndc	package	67777-010-03	openfda.package_ndc
ndc	package	67777-010-17	openfda.package_ndc
ndc	package	67777-010-14	openfda.package_ndc
ndc	package	67777-010-13	openfda.package_ndc
ndc	package	67777-010-11	openfda.package_ndc
ndc	package	67777-010-10	openfda.package_ndc
ndc	package	67777-010-05	openfda.package_ndc
ndc	package	67777-010-04	openfda.package_ndc
ndc	package	67777-010-16	openfda.package_ndc
ndc	package	67777-010-01	openfda.package_ndc
ndc	package	67777-010-06	openfda.package_ndc
ndc	product	67777-010	openfda.product_ndc
ndc11	package	67777001012	derived:openfda.package_ndc
ndc11	package	67777001002	derived:openfda.package_ndc
ndc11	package	67777001006	derived:openfda.package_ndc
ndc11	package	67777001013	derived:openfda.package_ndc
ndc11	package	67777001005	derived:openfda.package_ndc
ndc11	package	67777001014	derived:openfda.package_ndc
ndc11	package	67777001001	derived:openfda.package_ndc
ndc11	package	67777001019	derived:openfda.package_ndc
ndc11	package	67777001004	derived:openfda.package_ndc
ndc11	package	67777001010	derived:openfda.package_ndc
ndc11	package	67777001017	derived:openfda.package_ndc
ndc11	package	67777001015	derived:openfda.package_ndc
ndc11	package	67777001011	derived:openfda.package_ndc
ndc11	package	67777001018	derived:openfda.package_ndc
ndc11	package	67777001016	derived:openfda.package_ndc
ndc11	package	67777001020	derived:openfda.package_ndc
ndc11	package	67777001003	derived:openfda.package_ndc
rxcui		581662	openfda.rxcui

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 Do not use In the eyes. When using this product • Avoid contact with eyes. • In case of eye contact, rinse with water to remove Stop use and ask a doctor if Irritation and redness develop. 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.