NOT HAVE- antibacterial antiseptic spray spray

not have by

Drug Labeling and Warnings

not have by is a Otc medication manufactured, distributed, or labeled by Guangzhou Oumiao Cosmetics Co. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

Use

Antiseptic Spray to help reduce bacteria on the skin.

Warnings

1.Flammable,Keep away from fire or flame.

2.For external use only.

DO NOT USE

When using this product

do not use in or near the eyes. In case of contact,rinse eyes thorughly with water.

STOP USE

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

Keep out of reach of children

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

Directions

Place enough Product in your palm to cover hands and rub hands together briskyly until dry.

Children under 6 years of age should be supervised when using

Other information

Store below 110°F.(43℃)·

May discolor certain fabrics or surfaces.

Inactive ingredients

ALCOHOL(75%) , AQUA, POLYHEXAMETHYLENE BIGUANIDE HYDROCHLORIDE 0.36%-0.44%

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

NOT HAVE 
antibacterial antiseptic spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74761-002
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
WATER (UNII: 059QF0KO0R)
POLIHEXANIDE HYDROCHLORIDE (UNII: 4XI6112496)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74761-002-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
2	NDC: 74761-002-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
3	NDC: 74761-002-03	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
4	NDC: 74761-002-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
5	NDC: 74761-002-05	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
6	NDC: 74761-002-06	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
7	NDC: 74761-002-07	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
8	NDC: 74761-002-08	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
9	NDC: 74761-002-09	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
10	NDC: 74761-002-10	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
11	NDC: 74761-002-11	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
12	NDC: 74761-002-12	400000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
13	NDC: 74761-002-13	800000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
14	NDC: 74761-002-14	1000000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/04/2020

Labeler - Guangzhou Oumiao Cosmetics Co. Ltd. (529806412)

Registrant - Guangzhou Oumiao Cosmetics Co. Ltd. (529806412)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Oumiao Cosmetics Co. Ltd.		529806412	manufacture(74761-002)