ALCOHOL WET WIPES swab SANITIZING WIPE swab

Sanitizing Wipe by

Drug Labeling and Warnings

Sanitizing Wipe by is a Otc medication manufactured, distributed, or labeled by Suzhou Borage Medical Technology Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol 75% by volume................Antiseptic

INDICATIONS & USAGE

For hand washing to decrease bacteria on the skin.

Apply topically to the skin to help prevent cross contamination.

WARNINGS

• Flammable, keep away from fire or flame.
• For external only.
• When using this product do not use in or near the eyes. In case of contact. rinse eyes throughly with water.
• Stop and ask doctor If irritation or rash appears and lasts.
• Keep this out of reach of children. If swallowed. get medical help or contact a Poison Control Center right away.

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

PURPOSE

For hand washing to decrease bacteria on the skin.

DOSAGE & ADMINISTRATION

• Tear open packet
• Open and unfold wipe
• Thoroughly wipe hands, fingers and wrists.
• Discard after single use.

INACTIVE INGREDIENT

Water

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALCOHOL WET WIPES 
alcohol wet wipes swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78627-001
Route of Administration	TOPICAL, EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75   in 100

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78627-001-01	800 in 1 PACKAGE; Type 0: Not a Combination Product	06/01/2020
2	NDC: 78627-001-02	800 in 1 CANISTER; Type 0: Not a Combination Product	06/01/2020
3	NDC: 78627-001-03	50 in 1 BAG; Type 0: Not a Combination Product	09/28/2020
4	NDC: 78627-001-04	300 in 1 CANISTER; Type 0: Not a Combination Product	10/14/2020
5	NDC: 78627-001-05	150 in 1 CANISTER; Type 0: Not a Combination Product	10/14/2020
6	NDC: 78627-001-07	10 in 1 PACKAGE	01/14/2021
6	NDC: 78627-001-06	1 in 1 BAG; 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	06/01/2020

ALCOHOL WET WIPES 
alcohol wet wipes swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78627-206
Route of Administration	TOPICAL, EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67.8246 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78627-206-01	5 g in 1 PACKET; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

SANITIZING WIPE 
sanitizing wipe swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78627-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.115   in 100

Inactive Ingredients
Ingredient Name	Strength
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)
CHLORPHENESIN (UNII: I670DAL4SZ)
LAURYLPYRIDINIUM CHLORIDE (UNII: KJM5A6A3YL)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
WATER (UNII: 059QF0KO0R)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78627-003-01	1 in 1 PACKAGE; Type 0: Not a Combination Product	07/08/2020
2	NDC: 78627-003-02	10 in 1 PACKAGE; Type 0: Not a Combination Product	07/08/2020
3	NDC: 78627-003-03	20 in 1 PACKAGE; Type 0: Not a Combination Product	07/08/2020
4	NDC: 78627-003-04	40 in 1 PACKAGE; Type 0: Not a Combination Product	07/08/2020
5	NDC: 78627-003-05	80 in 1 PACKAGE; Type 0: Not a Combination Product	07/08/2020
6	NDC: 78627-003-06	100 in 1 PACKAGE; Type 0: Not a Combination Product	07/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/08/2020

Labeler - Suzhou Borage Medical Technology Co.,Ltd. (541550629)