NATURAL HOUSE HAND SANITIZER- hand sanitizer gel

Natural House Hand Sanitizer by

Drug Labeling and Warnings

Natural House Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Aquagenics Technologies, Pond Alliance Inc dba Aquagenics Technologies. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 62% Purpose: Antimicrobial

Purpose

Antimicrobial, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria on skin.

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

Avoid contact with eyes. In case of contact, rinse eyes 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.

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

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

Store below 40C (104F)

Inactive ingredients

purified water USP, glycerin, aloe, carbomer, lavender oil.

Package Label - Principal Display Panel

236 mL NDC: 73763-460-01

INGREDIENTS AND APPEARANCE

NATURAL HOUSE HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73763-460
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ALOE (UNII: V5VD430YW9)
WATER (UNII: 059QF0KO0R)
CARBOMER 940 (UNII: 4Q93RCW27E)
LAVENDER OIL (UNII: ZBP1YXW0H8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73763-460-01	236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/16/2020
2	NDC: 73763-460-02	473 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/16/2020
3	NDC: 73763-460-03	946 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/16/2020
4	NDC: 73763-460-04	1893 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/16/2020
5	NDC: 73763-460-05	3785 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/16/2020

Labeler - Pond Alliance dba Aquagenics Technologies (064752511)

Establishment
Name	Address	ID/FEI	Business Operations
Pond Alliance Inc dba Aquagenics Technologies		832675305	manufacture(73763-460)