FDA.reportPublic FDA data

NYC HEALTH HOSPITALS

Manufacturer
STRONGHOLD TRADING LLC | S-ONE PHARMACEUTICAL INC
Effective date
2022-01-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:16:20

Label at a glance#

ProductNYC HEALTH HOSPITALS
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin.

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using Safe Cleaner Hand Sanitizer.

Storage and handling

Store below 110F (43C) May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

DOSAGE & ADMINISTRATION SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame. For external use only

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

irritation or rash appears and lasts.

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

INDICATIONS & USAGE SECTION

Put enough product in your palm to cover hands and rub hands together briskly until dry.

Children under 6 years of age should be supervised when using Safe Cleaner Hand Sanitizer.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store below 110F (43C)

May discolor certain fabrics or surfaces.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Glycerine, Purified water, Propylene glycol, Carbomer, Triethanolamine, Sophora extract, Grapefruit seed extract, Mentha oil

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2ml NDC: 80969-050-012ml NDC: 80969-050-01

60ml NDC: 80969-050-0260ml NDC: 80969-050-02

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80969-05080969-050-01, 80969-050-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
PEPPERMINT OILAV092KU4JHIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT
CITRUS PARADISI SEED12F08874Y7IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f7d92e52-7930-5557-e053-6294a90aca91b4714640-261b-86ad-e053-2a95a90ad2972023-03-26WarningsExact identifier
spl set id: b4714640-261b-86ad-e053-2a95a90ad297

Reported adverse events (FAERS/openFDA)#

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