FDA.reportPublic FDA data

All Day Ultra Hand Sanitizer Gel

Manufacturer
General Resources LLC
Effective date
2020-10-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:09:54

Label at a glance#

ProductAll Day Ultra Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure14 sections

Storage and handling

Other information Store above 0°C (32°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 72%

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • Hand sanitizing to help reduce bacteria on the skin
  • Recommended for repeated use

WARNINGS SECTION

Warnings

For external use only

Flammable, keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

​Stop use and ask a doctor if irritation or redness appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

Apply liberally to hands and gently rub until dry.

STORAGE AND HANDLING SECTION

Other information

Store above 0°C (32°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients

purified water, isopropyl alcohol, glycerin, alpha-tocopherol acetate, aminomethylpropanol

OTC - QUESTIONS SECTION

Questions?Call 1-844-929-9199

SPL UNCLASSIFIED SECTION

Distributed by: General Resources, LLC

1430 Haines Avenue, Ste. 105-186

Rapid City, South Dakota 57701

www.alldayprotect.com

* Patented formula effectively eliminates 99.99% of harmful germs, bacteria and viruses in as little as 15 seconds; antimicrobial protection for up to 24 hours.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

24 HR

ALL DAY ULTRA

HAND SANITIZER GEL

ALCOHOL-BASED

INSTANTLY KILLS 99.99% OF TESTED GERMS*

FRAGRANCE-FREE

2 fl oz (60 mL)

Proudly made in the USA

AllDayUltra-gel-v3AllDayUltra-gel-v3

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70481-11270481-112-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302IACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
b299463c-2101-15f8-e053-2a95a90aa2069e54da7c-ca1d-6f5a-e053-2a95a90a53812020-10-26WarningsExact identifier
spl id: b299463c-2101-15f8-e053-2a95a90aa206
spl set id: 9e54da7c-ca1d-6f5a-e053-2a95a90a5381

Reported adverse events (FAERS/openFDA)#

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