Go PSP hand sanitizer by RW Consumer Products Ltd Go PSP hand sanitizer

Go PSP hand sanitizer by

Drug Labeling and Warnings

Go PSP hand sanitizer by is a Otc medication manufactured, distributed, or labeled by RW Consumer Products Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GO PSP HAND SANITIZER- isopropyl alcohol solution 
RW Consumer Products 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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Go PSP hand sanitizer

Drug Facts

Active ingredient

Isopropyl alcohol 70%

Purpose

Antiseptic

Use

• Helps reduce bacteria on the skin
• Recommended for repeated use

Warnings

Flammable, keep away from fire or flame.
For external use only.

When using this product

• Keep out of eyes 
• In case of contact with eyes, flush thoroughly with water
• Avoid contact with broken skin 
• Do not inhale or ingest

Stop use and ask a doctor if

• Irritation and redness develop and persist for more than 72 hours

Keep out of reach of children.

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

Directions

• Spray directly on hands and rub in thoroughly over 30 seconds
• Allow to dry
• For children under 6, use adult supervision 
• Not recommended for infants

Other Information

• Do not store above 104°F/40°C
• Do not use if shrink band around cap is broken or missing

Inactive ingredients

glycerin, hydrogen peroxide, purified water

Package Labeling:

GO PSP HAND SANITIZER 
isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69612-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69612-011-01	1 in 1 BOX	10/01/2021	05/20/2022
1		100 mL in 1 BOTTLE, SPRAY; 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	part333E	10/01/2021	05/20/2022

Labeler - RW Consumer Products Ltd (245592118)

Revised: 5/2022

Document Id: df736abd-9cee-4e90-e053-2995a90aab5e

34390-5

Set id: cba66231-f8a0-2d03-e053-2a95a90a29ce

Version: 2

Effective Time: 20220520