Goop Hydro-Gel

Manufacturer: Critzas Industries, Inc.
Effective date: 2020-07-29
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:23:34

Label at a glance#

ProductGoop Hydro-Gel

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age
on open skin wounds

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredient

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Goop Hand Sanitizer

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
23058-1008-1	2022-01-28	C162847	48780-1	d6a99b39-4420-a426-e053-dadaa90af4c2	ab9a7085-a4f2-612f-e053-2995a90ab246
23058-1008-2	2022-01-28	C162847	48780-1	d6a99b39-4420-a426-e053-dadaa90af4c2	ab9a7085-a4f2-612f-e053-2995a90ab246

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
23058-1008-1	Goop Hydro-Gel	250 mL in 1 BOTTLE, DISPENSING	GEL	250		1
23058-1008-2	Goop Hydro-Gel	500 mL in 1 BOTTLE, DISPENSING	GEL	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
23058-1008	GOOP HYDRO-GEL (ALCOHOL) GEL [CRITZAS INDUSTRIES, INC.]	1	Legacy NDC, 2 package rows	20200803_ab9a7085-a4f2-612f-e053-2995a90ab246.zip

Products#

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

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

Goop Hydro-Gel
ALCOHOL
GLYCERIN
HYDROXYPROPYL CELLULOSE, UNSPECIFIED
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
23058-1008	23058-1008-1, 23058-1008-2

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
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIED	9XZ8H6N6OH	IACT
WATER	059QF0KO0R	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
ab9a4bee-1334-3009-e053-2a95a90a3ef7			ab9a7085-a4f2-612f-e053-2995a90ab246	2020-07-29	Warnings	Exact identifier spl id: ab9a4bee-1334-3009-e053-2a95a90a3ef7 spl set id: ab9a7085-a4f2-612f-e053-2995a90ab246

Reported adverse events (FAERS/openFDA)#

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