NATURE HAND SANITIZER- ethyl alcohol gel

NATURE HAND SANITIZER by

Drug Labeling and Warnings

NATURE HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Snt Wholesale, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active Ingredients

Ethyl Alcohol 80% (v/v)

Purpose

Antiseptic

Uses

• Hand Sanitizer to help reduce bacteria that potentially can cause disease. Recommended for repeated use.
• For use when soap and water are not available.

Warnings

Flammable. Keep away from fire or flame.

For external use only: hands

When using this product ▪ Keep out of eyes, ears and mouth. ▪ In case of contact with eyes, rinse eyes thoroughly with water. ▪ Do not inhale or ingest.

Do not use ▪ In children less than 2 months of age. ▪ On open skin wounds.

Stop use and ask a doctor if ▪ Irritation or rash & redness develops. ▪ These may be signs of a serious condition. ▪ Condition persist for more than 72 hours.

Keep out of reach of children. ▪ If swallowed, get medical help immediately. ▪ Contact a Poison Control Centre right away.

Directions

▪ Apply enough product to cove hand thoroughly. ▪ Rub hands together, until hands feel dry, Do not rinse. ▪ Children under 6 years of age should be supervised when using this product. ▪ Not recommended for infants.

Other information

▪ Store below 105°F (40°C). May discolor some fabrics
▪ Avoid freezing and excessive heat above 105°F (40°C).

Inactive ingredients

Aqua (Water), Glycerin, Propylene Glycol, Fragrance (Parfum), Carbomer, Aloe Barbadensis Leaf Extract, Triethanolamine.

SPL UNCLASSIFIED SECTION

Contains 80% Alcohol

Infused with Aloe

Distributed by:

SNT WHOLESALE INC.

5102 Frolich In, Hyattsville,

MD 20781 USA.

Tel: +1-240-423-3875

www.sntwholesale.com

MFG. DT.   : 06/2020

EXP. DT.    : 05/2023

BATCH NO.: HS 038

PLEASE RECYCLE

Made In India

Packaging

INGREDIENTS AND APPEARANCE

NATURE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78914-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78914-000-12	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2020
2	NDC: 78914-000-25	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2020
3	NDC: 78914-000-50	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2020
4	NDC: 78914-000-10	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/15/2020

Labeler - Snt Wholesale, Inc. (117545607)