HUGO NATURALS VANILLA PEPPERMINT HAND SANITIZER- ethanol spray 
Dm Natural Products, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

HUGO Naturals VANILLA PEPPERMINT HAND SANITIZER

Drug Facts

Active Ingredients

Ethanol* 62%

Purpose 

Antimicrobial

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

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. 

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

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 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

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

image description

HUGO NATURALS  VANILLA PEPPERMINT HAND SANITIZER
ethanol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70279-610
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALLANTOIN (UNII: 344S277G0Z)  
HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70279-610-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product12/29/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A12/29/2015
Labeler - Dm Natural Products, Inc. (623230898)

Revised: 7/2017
Document Id: 5468b804-3364-49e1-ab2b-ed52e997cd2a
Set id: 2d6bc34b-1919-4fa4-941a-8217ec378973
Version: 1
Effective Time: 20170705
 
Dm Natural Products, Inc.