FDA.reportPublic FDA data

New Horizon Hand Sanitizer

Manufacturer
Sokol and Company
Effective date
2020-12-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:02:57

Label at a glance#

ProductNew Horizon Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

to decrease bacteria on the skin

Dosage and administration

apply liberally to hands to cover all surfaces rub hands together until dry supervise children under 6 years old not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from fire or flame

When using this product

OTC - WHEN USING SECTION

keep away from eyes. In case of eye contact, rinse eyes with water.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation or redness develop or last more than 72 hours

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally to hands to cover all surfaces
  • rub hands together until dry
  • supervise children under 6 years old
  • not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

  • store between 15-30C (59-86F)
  • avoid freezing and excessive heat above 40 C (104 F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, methylcellulose, purified water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81215-00081215-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
METHYLCELLULOSE, UNSPECIFIEDZ944H5SN0HIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
cc81b631-bd77-1f68-e053-2a95a90a1146b60bda65-7349-3680-e053-2a95a90a732c2021-09-21WarningsExact identifier
spl set id: b60bda65-7349-3680-e053-2a95a90a732c

Reported adverse events (FAERS/openFDA)#

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