HUGO NATURALS FRENCH LAVENDER HAND SANITIZER- ethanol spray

HUGO Naturals by

Drug Labeling and Warnings

HUGO Naturals by is a Otc medication manufactured, distributed, or labeled by Dm Natural Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Ethanol* 62%

Purpose

Antimicrobial

INDICATIONS & USAGE

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

WARNINGS

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.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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

Inactive Ingredients: Aqua/Water, Glycerin, 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

INGREDIENTS AND APPEARANCE

HUGO NATURALS  FRENCH LAVENDER HAND SANITIZER
ethanol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70279-293
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALLANTOIN (UNII: 344S277G0Z)
HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
LAVENDER OIL (UNII: ZBP1YXW0H8)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70279-293-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/29/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/29/2015

Labeler - Dm Natural Products, Inc. (623230898)