ALCOHOL WET WIPES- alcohol wet wipes swab 
SANITIZING WIPE- sanitizing wipe swab 
Suzhou Borage Medical Technology 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.

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

For hand washing to decrease bacteria on the skin.

Apply topically to the skin to help prevent cross contamination.

  • 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.

For hand washing to decrease bacteria on the skin.

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

Water

Label

Sanitizing Wipe

800pc

50pack/bag

300/canister

1 swab single bag

10 bag per package

ALCOHOL WET WIPES 
alcohol wet wipes swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78627-001
Route of AdministrationTOPICAL, EXTRACORPOREAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75   in 100 
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
WATER (UNII: 059QF0KO0R)  
ALOE (UNII: V5VD430YW9)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78627-001-01800 in 1 PACKAGE; Type 0: Not a Combination Product06/01/2020
2NDC:78627-001-02800 in 1 CANISTER; Type 0: Not a Combination Product06/01/2020
3NDC:78627-001-0350 in 1 BAG; Type 0: Not a Combination Product09/28/2020
4NDC:78627-001-04300 in 1 CANISTER; Type 0: Not a Combination Product10/14/2020
5NDC:78627-001-05150 in 1 CANISTER; Type 0: Not a Combination Product10/14/2020
6NDC:78627-001-0710 in 1 PACKAGE01/14/2021
6NDC:78627-001-061 in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/01/2020
ALCOHOL WET WIPES 
alcohol wet wipes swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78627-206
Route of AdministrationTOPICAL, EXTRACORPOREAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL67.8246 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78627-206-015 g in 1 PACKET; Type 0: Not a Combination Product06/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/01/2020
SANITIZING WIPE 
sanitizing wipe swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78627-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.115   in 100 
Inactive Ingredients
Ingredient NameStrength
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
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78627-003-011 in 1 PACKAGE; Type 0: Not a Combination Product07/08/2020
2NDC:78627-003-0210 in 1 PACKAGE; Type 0: Not a Combination Product07/08/2020
3NDC:78627-003-0320 in 1 PACKAGE; Type 0: Not a Combination Product07/08/2020
4NDC:78627-003-0440 in 1 PACKAGE; Type 0: Not a Combination Product07/08/2020
5NDC:78627-003-0580 in 1 PACKAGE; Type 0: Not a Combination Product07/08/2020
6NDC:78627-003-06100 in 1 PACKAGE; Type 0: Not a Combination Product07/08/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/08/2020
Labeler - Suzhou Borage Medical Technology Co.,Ltd. (541550629)

Revised: 1/2021
Document Id: b8d3ac2d-fb46-bd09-e053-2a95a90a5eb8
Set id: a702125f-2f0a-4c53-e053-2995a90ad724
Version: 7
Effective Time: 20210113
 
Suzhou Borage Medical Technology Co.,Ltd.