Zhejiang Qimei-GoodEarth BZK wipes 1000 PCS

GoodEarth by

Drug Labeling and Warnings

GoodEarth by is a Otc medication manufactured, distributed, or labeled by Zhejiang Qimei Commodity Co. Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GOODEARTH- sanitizing wipes swab 
Zhejiang Qimei Commodity Co. Ltd

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Zhejiang Qimei-GoodEarth BZK wipes 1000 PCS

Active Ingredient(s)

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

in or near the eyes.
on open skin wounds or burns

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

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

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

Directions

• Apply to hands and skin. No rinsing required. Discard after use.
• Children under 6 years of age should be supervised when using this product.

Other information

• Avoid freezing and store below 110F (43C).
• Dispose the used wipe in trash, do not flush it into the toilet.
• May discolor certain fabrics or surfaces.

Inactive ingredients

aloe babadensis leaf juice, decyl glucoside, glycerin, water.

Package Label - Principal Display Panel

1000 mL NDC: 69821-223-01

GOODEARTH 
sanitizing wipes swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69821-223
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69821-223-01	1000 in 1 BAG	06/20/2020	11/09/2020
1		1000 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/20/2020	11/09/2020

Labeler - Zhejiang Qimei Commodity Co. Ltd (544331136)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Qimei Commodity Co. Ltd		544331136	manufacture(69821-223)

Revised: 11/2020

Document Id: b3af93c7-457d-802e-e053-2995a90a6b39

34390-5

Set id: a8e8f82e-6330-91b2-e053-2a95a90a3490

Version: 3

Effective Time: 20201109