NERF Hand Sanitizer

Manufacturer: Gold Orient International Limited
Effective date: 2020-07-16
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:22:11

Label at a glance#

ProductNERF Hand Sanitizer NERF 200

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping.

Storage and handling

Store at 68 to 77F (20-25C) Do not store above 110F(43C) You may report a serious adverse reaction to this product to Report Reaction, LLC, PO Box 22, Plainsboro, NJ 08536

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat. 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire and flames.

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.

Other information

STORAGE AND HANDLING SECTION

Store at 68 to 77F (20-25C)
Do not store above 110F(43C)
You may report a serious adverse reaction to this product to Report Reaction, LLC, PO Box 22, Plainsboro, NJ 08536

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,

Glycerin,

Acrylates/C10-30 Alkyl Acrylate Crosspolymer,

Fragrance,

Polysorbate 20,

Sodium Hydroxide,

Yellow 5,

Blue 1

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	1
581660	ethanol 0.62 ML/ML Topical Gel	SCD	1
581660	ethanol 62 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51522-025-01	2022-01-28	C162847	48780-1	d6a99b39-770b-a426-e053-dadaa90af4c2	NERF(NERF 200)Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51522-025-01	NERF Hand SanitizerNERF 200	89 mL in 1 BOTTLE, PLASTIC	GEL	89		1
51522-025-01	NERF Hand SanitizerNERF 200	1 in 1 POUCH	GEL	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51522-025	NERF HAND SANITIZER NERF 200 (ALCOHOL) GEL [GOLD ORIENT INTERNATIONAL LIMITED]	1	Legacy NDC, 2 package rows	20200722_aa9b7953-a514-1fe0-e053-2995a90a7ec7.zip

Products#

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

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

NERF Hand Sanitizer NERF 200
Alcohol
POLYSORBATE 20
SODIUM HYDROXIDE
FD&C BLUE NO. 1
GLYCERIN
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
FD&C YELLOW NO. 5
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51522-025	51522-025-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
POLYSORBATE 20	7T1F30V5YH	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
WATER	059QF0KO0R	IACT

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
aa9b7953-a515-1fe0-e053-2995a90a7ec7			aa9b7953-a514-1fe0-e053-2995a90a7ec7	2020-07-16	Warnings	Exact identifier spl id: aa9b7953-a515-1fe0-e053-2995a90a7ec7 spl set id: aa9b7953-a514-1fe0-e053-2995a90a7ec7

Reported adverse events (FAERS/openFDA)#

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