gumdrop glitz hand sanitizer

Manufacturer: Target Corporation
Effective date: 2023-10-26
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 23:57:52

Label at a glance#

Productgumdrop glitz hand sanitizer

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hand-washing to decrease bacteria on the skin, only when water is not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flames

For external use only

When using this product

OTC - WHEN USING SECTION

do not get into eyes.
if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop

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

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, fragrance, triethanolamine, denatonium benzoate

SPL UNCLASSIFIED SECTION

not tested on animals

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelBox

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	4
581660	ethanol 0.62 ML/ML Topical Gel	SCD	4
581660	ethanol 62 % Topical Gel	SY	4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11673-868-30	gumdrop glitz hand sanitizer	30 g in 1 BOTTLE, PLASTIC	GEL	30		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-868	GUMDROP GLITZ HAND SANITIZER (ALCOHOL) GEL [TARGET CORPORATION]	4	Current NDC, Legacy NDC, 1 package rows	20231026_c1731db5-34ac-4773-a99b-ac4eae7ab433.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

gumdrop glitz hand sanitizer
ALCOHOL
WATER
GLYCERIN
TROLAMINE
DENATONIUM BENZOATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11673-868	11673-868-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
TROLAMINE	9O3K93S3TK	IACT
DENATONIUM BENZOATE	4YK5Z54AT2	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
gumdrop glitz hand sanitizer	ALCOHOL	Target Corporation	c1731db5-34ac-4773-a99b-ac4eae7ab433	2023-10-26	Warnings	Exact identifier ndc (package): 11673-868-30 ndc (product): 11673-868 ndc11 (package): 11673086830 spl id: 089971c6-98d8-a75b-e063-6394a90a6a84 spl set id: c1731db5-34ac-4773-a99b-ac4eae7ab433

Reported adverse events (FAERS/openFDA)#

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