What a Complete Shit Show Hand Sanitizer

What a Complete Shit Show Hand Sanitizer by

Drug Labeling and Warnings

What a Complete Shit Show Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Blue Q. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WHAT A COMPLETE SHIT SHOW HAND SANITIZER- alcohol gel 
Blue Q

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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What a Complete Shit Show Hand Sanitizer

Drug Facts

Active ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic Handwash

Uses

For handwashing to decrease bacteria on the skin.

Warnings

For external use only. Flammable. Keep away from fire and flame.

When using this product

When using this product do not use in the eyes. In case of contact with eyes, rinse eyes with water.

Stop use and ask a doctor

Stop use and ask a doctor if irritation and redness develops and persists.

Keep out of reach of children

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

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Other information

Store under 105°F

Inactive ingredients

Water (Aqua), vegetable glycerin, isopropyl myristate, aloe vera, carbomer, fragrance

What a Complete Shit Show Hand Sanitizer

HAND SANITIZER

2 fl oz (59 ml)

Manufactured for Blue Q

703 West Housatonic St.

Pittsfield, MA 01201

WHAT A COMPLETE SHIT SHOW HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65194-632
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65194-632-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020	10/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/01/2020	10/31/2023

Labeler - Blue Q (192841674)

Revised: 1/2023

Document Id: eff7ef0c-21e0-064d-e053-2995a90a5978

34390-5

Set id: a838b4b4-fa08-5efa-e053-2995a90a7976

Version: 2

Effective Time: 20230102