ROADPRO Hand Sanitizer Foaming by Xiamen Wally Bath Manufacture Co., Ltd

ROADPRO Hand Sanitizer Foaming by

Drug Labeling and Warnings

ROADPRO Hand Sanitizer Foaming by is a Otc medication manufactured, distributed, or labeled by Xiamen Wally Bath Manufacture Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ROADPRO HAND SANITIZER FOAMING- alcohol liquid 
Xiamen Wally Bath Manufacture Co., Ltd

----------

Active Ingredient(s)

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

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 children less than 2 months of age
  • on open skin wounds

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

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

glycerin, PEG-10 Dimethicone, purified water USP, Chlorhexidine digluconate, Fragrance (Parfum)

Package Label - Principal Display Panel

250 mL NDC: 78868-004-01

hand sanitizer foaming 250ml label

ROADPRO HAND SANITIZER FOAMING 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78868-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX) 2.5 mL  in 100 mL
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) 4 mL  in 100 mL
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78868-004-01250 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00303/30/202012/01/2023
Labeler - Xiamen Wally Bath Manufacture Co., Ltd (548232606)
Establishment
NameAddressID/FEIBusiness Operations
Xiamen Wally Bath Manufacture Co., Ltd548232606manufacture(78868-004)

Revised: 7/2024