FDA.reportPublic FDA data

Choice Hand Sanitizing Gel 183

Manufacturer
Inopak. Ltd
Effective date
2023-02-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:36:16

Label at a glance#

ProductChoice Hand Sanitize
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Keep out of reach of children

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 right away. Children should be supervised by an adult when using this product.

Usage

INDICATIONS & USAGE SECTION

Uses

  • To decrease bacteria on the skin that potentially can cause disease
  • Recommended for repeated use

Warnings

WARNINGS SECTION

Warnings

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

Other Information

OTHER SAFETY INFORMATION

Keep out of eyes, ears or mouth. In case of eye contact, flush eyes with water

May discolor certain fabrics and surfaces.

Stop Usage

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop or if condition persists for more than 72 hours.

Administration

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply sufficient amount of product to your palm to cover both hands.
  • Rub until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C 10/30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, FD&C Blue 1, FD&C Yellow 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E, Water

Choice Box Container

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug Facts

Active Ingredient                             Purpose

Ethyl Alcohol 70% v/v ……………Antiseptic

Uses

  • To decrease bacteria on the skin that potentially can cause disease
  • Recommended for repeated use

Warnings

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

Keep out of eyes, ears or mouth. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation and redness develop or if condition persists for more than 72 hours.

Keep out of reach of children. If swallowed. Get medical help or contact a Poison Control Center right away. Children should be supervised by an adult when using this product.

Directions

  • Apply sufficient amount of product to your palm to cover both hands.
  • Rub until dry.

Other Information

May discolor certain fabrics and surfaces.

Inactive Ingredients

Acrylates/C 10/30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, FD&C Blue 1, FD&C Yellow 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E, Water

Choice

HAND SANITIZING GEL

Aloe Ver

  And

Vitamin E

Instant

Waterless

Contains

Moisturizers

PN 5025-404UV-CH

800m 

Hand sanitizing gel

  • Contains Aloe Vera and Vitamin E
  • Instant waterless with moisturizers
  • Produced in an FDA registered facility
  • cGMP facility
  • Dries quickly leaving the skin feeling soothed and moisturized

Kills

99.9% of

Germs

MADE IN THE USA

Choice

Dispenser Loading Instructions

Section 1Section 1Section 2Section 2Section 3Section 3Section 4Section 4

      Section 1                                 Section 2                           Section 3                           Section 4

Choice BoxChoice Box

Choice Case

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

                                                                                5025-CH-CS         Rev. 1.0

Choice™

HAND SANITIZING GEL                   Kills 99.9% of Germs

Instant Waterless                             Aloe Ver and Vitamin E

Contains Moisturizers

MADE IN THE USA                           5025-404UV-CH

                                                                12/800 ML UV                   040232 65077 2

Choice CaseChoice Case

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58575-183-012023-02-19C16284748780-1f386c64a-410f-0266-e053-dadaa90a7c1aChoice Hand Sanitizing Gel 183
58575-183-022023-02-19C16284748780-1f386c64a-410f-0266-e053-dadaa90a7c1aChoice Hand Sanitizing Gel 183
58575-183-012023-01-30C16284748780-1f386c64a-410f-0266-e053-dadaa90a7c1aChoice Hand Sanitizing Gel 183
58575-183-022023-01-30C16284748780-1f386c64a-410f-0266-e053-dadaa90a7c1aChoice Hand Sanitizing Gel 183

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58575-18358575-183-01, 58575-183-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOEV5VD430YW9IACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
ISOPROPYL ALCOHOLND2M416302IACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
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
f51751ff-fab2-aaf1-e053-2995a90a5a8e0e79d928-6c3d-45e6-bdef-a13fec91fe642023-02-19WarningsExact identifier
spl id: f51751ff-fab2-aaf1-e053-2995a90a5a8e
spl set id: 0e79d928-6c3d-45e6-bdef-a13fec91fe64

Reported adverse events (FAERS/openFDA)#

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