BIOARMOUR HAND SANITIZER SQUEEZE HOSE- alcohol gel

BioArmour Hand Sanitizer by

Drug Labeling and Warnings

BioArmour Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ningbo Pretty Tourism Manufacturer Co. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 70% Purpose: Antimicrobial

Purpose

Antimicrobial

Uses

Use(s)

• For handwashing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

Warnings

For external use only. Flammable, keep away from heat and flame.

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

STOP USE

• Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wet hands thoroughly with product
• Briskly rub hands together until dry
• Supervise children under 6 years in the use of this product

Other information

• Store at 20 oC to 25 oC (68 o to 77 oF)
• May discolor certain fabrics

Inactive ingredients

Water (aqua), Triethanolamine, Carbomer, Propylene Glycol, Glycerin, Aloe Barbadensis Extract, Tocopheryl Acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BIOARMOUR HAND SANITIZER  SQUEEZE HOSE
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75749-001
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
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75749-001-01	30 mL in 1 TUBE; Type 0: Not a Combination Product	04/28/2020
2	NDC: 75749-001-02	60 mL in 1 TUBE; Type 0: Not a Combination Product	04/28/2020
3	NDC: 75749-001-03	80 mL in 1 TUBE; Type 0: Not a Combination Product	04/28/2020
4	NDC: 75749-001-04	100 mL in 1 TUBE; Type 0: Not a Combination Product	04/28/2020
5	NDC: 75749-001-05	120 mL in 1 TUBE; Type 0: Not a Combination Product	04/28/2020
6	NDC: 75749-001-06	150 mL in 1 TUBE; Type 0: Not a Combination Product	04/28/2020
7	NDC: 75749-001-07	180 mL in 1 TUBE; Type 0: Not a Combination Product	04/28/2020
8	NDC: 75749-001-08	200 mL in 1 TUBE; Type 0: Not a Combination Product	04/28/2020
9	NDC: 75749-001-09	250 mL in 1 TUBE; Type 0: Not a Combination Product	04/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/28/2020

Labeler - Ningbo Pretty Tourism Manufacturer Co. Ltd. (553193489)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Pretty Tourism Manufacturer Co. Ltd.		553193489	manufacture(75749-001)