HandSanitizerGelBloodOrange

Manufacturer: Naturich Labs, Inc
Effective date: 2025-12-30
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 01:29:34

Label at a glance#

ProductHandSanitizerGelBloodOrange

Active ingredientALCOHOL

Label structure11 sections

Indications and uses

Helps decrease bacteria on skin. Recommended for repeated use

Dosage and administration

Squeeze a small drop onto palms and rub together. For children under 6 years, use adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

Helps decrease bacteria on skin. Recommended for repeated use

Warnings

WARNINGS SECTION

Flammable: keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

- Keep out of eyes

- In case of contact with eyes, flush thoroughly with water.

- Avoid contact with broken skin

Stop Use

OTC - STOP USE SECTION

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

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 Immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

Squeeze a small drop onto palms and rub together. For children under 6 years, use adult supervision. Not recommended for infants.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Propanediol, Aloe Barbadensis (Aloe Vera) Leaf Juice, Caprylic/Capric Triglyceride, Cocos Nucifera (Coconut) Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Helianthus Annuus (Sunflower) Seed Oil, Lavandula Angustifolia (Lavender) Flower Extract, Natural Fragrance*, Aminomethyl Propanol, Carbomer, Citrus Aurantium Bergamia (Bergamo!) Fruit Oil, Tocopheryl Acetate, Citral, Limonene, Linalool.

Other Information:

OTHER SAFETY INFORMATION

Store between 16-30C (59-86F).

Avoid freezing and excessive heat above 40C (104F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GC Sanitizer Gel Back Panel

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

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0819978029599	GTIN-13: 0819978029599 EAN-13: 0819978029599 GTIN-12: 819978029599 UPC-A: 819978029599 GTIN storage (14 digits): 00819978029599	GC Sanitizer Gel Back Panel.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72496-1130-1	HandSanitizerGelBloodOrange	59.1 mL in 1 BOTTLE, PUMP	GEL	59.1		4
72496-1130-2	HandSanitizerGelBloodOrange	221.8 mL in 1 BOTTLE, PUMP	GEL	221.8		4

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

HandSanitizerGelBloodOrange
GC-Hand Sanitizer Gel-Blood Orange
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72496-1130	72496-1130-1, 72496-1130-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
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
HandSanitizerGelBloodOrange	GC-HAND SANITIZER GEL-BLOOD ORANGE	Naturich Labs, Inc	fc628374-4794-0d31-e053-6394a90af64a	2025-12-30	Warnings	Exact identifier ndc (package): 72496-1130-2 ndc (package): 72496-1130-1 ndc (product): 72496-1130 ndc11 (package): 72496113002 ndc11 (package): 72496113001 spl id: 47332489-08c3-bbc9-e063-6394a90a2b00 spl set id: fc628374-4794-0d31-e053-6394a90af64a

Reported adverse events (FAERS/openFDA)#

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