HAND SANITIZER GEL- alcohol solution

Hand Sanitizer Gel by

Drug Labeling and Warnings

Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by Rapid Cure Technologies INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 70% by volume. Purpose: Antiseptic

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

If swallowed, get medical help or contact a Poison Control Center right away.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Water (Aqua), Aloe Vera, Propylene Glycol, Carboxethyl Acrylate Crosspolymer, Fragrance, FD&C Blue #1, FD&C Yellow #5

DESCRIPTION

Hand Sanitizer Gel

Moisturizing with Aloe

Kills Harmful Bacteris and Germs

Non-sterile Solution.

Alcohol Antiseptic 70%

Topical Solution

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PRINCIPAL DISPLAY PANEL

1892 ML NDC: 75722-004-04

INGREDIENTS AND APPEARANCE

HAND SANITIZER GEL 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75722-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMMONIUM ACRYLOYLDIMETHYLTAURATE (UNII: KBC00G95HI)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
HEPTANAL (UNII: 92N104S3HF)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75722-004-01	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
2	NDC: 75722-004-02	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
3	NDC: 75722-004-03	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
4	NDC: 75722-004-04	1892 mL in 1 JUG; Type 0: Not a Combination Product	05/01/2020
5	NDC: 75722-004-05	3785 mL in 1 JUG; Type 0: Not a Combination Product	05/01/2020
6	NDC: 75722-004-06	18927 mL in 1 CONTAINER; Type 0: Not a Combination Product	05/01/2020
7	NDC: 75722-004-07	208198 mL in 1 DRUM; Type 0: Not a Combination Product	05/01/2020
8	NDC: 75722-004-08	1003025 mL in 1 CONTAINER; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

Labeler - Rapid Cure Technologies INC (017489374)