ALCOHOL INSTANT HAND SANITIZER gel

75% Alcohol Instant Hand Sanitizer by

Drug Labeling and Warnings

75% Alcohol Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Cannapresso Health. Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75%

Purpose

Antiseptic

Use

To decrease bacteia on the skin. Recommended for repeated use

Warnings

Do not use

Do not use in or around the eyes.

Keep out of reach for children.

WHEN USING

Do not use in or around the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts. Keep out of reach for children.

STOP USE

Stop use and ask doctor if irritation or rash appears and lasts.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach for children.

Directions

1, Place enough product in you palm to thoroughly spread on both hands and rub into the skin until dry.
2, Children under 6 years of age should be supervised when using this product.

Other information

1, Store below 106F(41°C).
2, May discolor certain fabrics or surfaces.

Inactive ingredients

Water,Carbomer,Triethanolamine,Lavander oil

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ALCOHOL INSTANT HAND SANITIZER 
alcohol instant hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75242-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LAVENDER OIL (UNII: ZBP1YXW0H8)
CARBOMER 1342 (UNII: 809Y72KV36)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75242-006-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 75242-006-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 75242-006-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 75242-006-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
5	NDC: 75242-006-05	119 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
6	NDC: 75242-006-06	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
7	NDC: 75242-006-07	149 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
8	NDC: 75242-006-08	199 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
9	NDC: 75242-006-09	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
10	NDC: 75242-006-10	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
11	NDC: 75242-006-11	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
12	NDC: 75242-006-12	349 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
13	NDC: 75242-006-13	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
14	NDC: 75242-006-14	499 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
15	NDC: 75242-006-15	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
16	NDC: 75242-006-16	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - Cannapresso Health. Inc. (117477763)

Establishment
Name	Address	ID/FEI	Business Operations
Cannapresso Health. Inc.		117477763	manufacture(75242-006)