HUGO Naturals

Manufacturer: Dm Natural Products, Inc.
Effective date: 2017-07-05
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:51:54

Label at a glance#

ProductHUGO Naturals VANILLA PEPPERMINT HAND SANITIZER

Active ingredientALCOHOL

Label structure9 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethanol* 62%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Uses Helps reduce bacteria on the skin. Recommended for repeated use.

WARNINGS SECTION

Warnings For external use only. Flammable, keep away from heat or flame. Do not use in or near eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation develops and persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away. Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions Spray in your palm and rub thoroughly to cover both hands. Briskly rub hands together until dry. Supervise children under 6 when using this product.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aqua/Water, Mentha Piperita (Peppermint) Oil, Glycerin, Natural Fragrance Oils, Allantoin, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Lavandula Angustifolia (Lavender) Oil, Aloe Barbadensis Leaf Juice.*

*Certified Organic

SPL UNCLASSIFIED SECTION

Moisturizing

Natural

Sulfate-free

Gluten-free

Soy-free

No Animal Testing

Recyclable

MADE IN THE USA for:

DM Natural Products, Inc.

Chatsworth, CA 91311

HugoNaturals.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1020364	ethanol 62 % Topical Spray	PSN	1
1020364	ethanol 0.62 ML/ML Topical Spray	SCD	1
1020364	ethanol 62 % Topical Spray	SY	1
1020364	ethyl alcohol 62 % Topical Spray	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70279-610-02	2020-01-31	C162847	48780-1	9d75b9d1-0f39-f424-e053-dadaa90a57ce	HUGO Naturals VANILLA PEPPERMINT HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70279-610-02	HUGO NaturalsVANILLA PEPPERMINT HAND SANITIZER	60 mL in 1 BOTTLE	SPRAY	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70279-610	HUGO NATURALS VANILLA PEPPERMINT HAND SANITIZER (ETHANOL) SPRAY [DM NATURAL PRODUCTS, INC.]	1	Legacy NDC, 1 package rows	20170712_2d6bc34b-1919-4fa4-941a-8217ec378973.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

HUGO Naturals VANILLA PEPPERMINT HAND SANITIZER
ETHANOL
ALCOHOL
WATER
PEPPERMINT OIL
GLYCERIN
ALLANTOIN
HAMAMELIS VIRGINIANA LEAF
LAVENDER OIL
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70279-610	70279-610-02

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
WATER	059QF0KO0R	IACT
PEPPERMINT OIL	AV092KU4JH	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALLANTOIN	344S277G0Z	IACT
HAMAMELIS VIRGINIANA LEAF	T07U1161SV	IACT
LAVENDER OIL	ZBP1YXW0H8	IACT
ALOE VERA LEAF	ZY81Z83H0X	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
5468b804-3364-49e1-ab2b-ed52e997cd2a			2d6bc34b-1919-4fa4-941a-8217ec378973	2017-07-05	Warnings	Exact identifier spl id: 5468b804-3364-49e1-ab2b-ed52e997cd2a spl set id: 2d6bc34b-1919-4fa4-941a-8217ec378973

Reported adverse events (FAERS/openFDA)#

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