SANITECT HAND SANITIZER- alcohol gel

Sanitect Hand Sanitizer by

Drug Labeling and Warnings

Sanitect Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Aquagenics Technologies. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 70%. Purpose: Hand Sanitizer

Purpose

Antimicrobal, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria on skin.

Warnings

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

WHEN USING

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Avoid contact with eyes. In case of contact, flush thoroughly with water. Do not inhale or ingest. Avoid contact with broken skin.

Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

STOP USE

Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

Apply product onto hands, briskly rub hands together until dry without wiping. For children under 6, use only under adult supervision.

Other information

Safe for repeated use.

Supervise children under 6 years of age.

Store at a temperature below 110F.

Inactive ingredients

Purified water, Glycerin, PEG-6 (and) AMP-Acrylates/Vinyl Isodecanoate Crosspolymer, Aloe, Fragrance.

Package Label - Principal Display Panel

236 mL NDC: 73763-470-01

INGREDIENTS AND APPEARANCE

SANITECT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73763-470
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
GLYCERIN (UNII: PDC6A3C0OX)
ALOE (UNII: V5VD430YW9)
WATER (UNII: 059QF0KO0R)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73763-470-01	236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/01/2020
2	NDC: 73763-470-02	473 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/01/2020
3	NDC: 73763-470-03	946 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/01/2020
4	NDC: 73763-470-04	1893 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/01/2020
5	NDC: 73763-470-05	3785 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/01/2020

Labeler - Aquagenics Technologies (064752511)