Red Devil Hand Sanitizer by Carrollclean LLC / Carrollclean Red Devil Hand Sanitizer

Red Devil Hand Sanitizer by

Drug Labeling and Warnings

Red Devil Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Carrollclean LLC, Carrollclean. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

RED DEVIL HAND SANITIZER- alcohol spray 
Carrollclean LLC

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.

----------

Red Devil Hand Sanitizer

Active Ingredients

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

*To sanitize hands without requiring water or a rinse

*Kills 99.9% of most common bacteria in 15 seconds.

Warnings

FLAMMABLE

For Extermal use only

When using this product

*Do not use near heat or flame.

*Do not use in or near eyes.

*Discontinue use if irritation and redness develop.

*Do not use on deep or puncture wounds, consult

your doctor.

Keep out of reach of children.

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

*Apply liberally to unsoiled hands and rub in thoroughly.

*Allow to dry without wiping or rinsing.

Other Information

Store at room temperature.

Inactive ingredients

Water, Glycerin, Isopropyl Myristate

Product Label

RED DEVIL HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73708-684
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70.5 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.22 mL  in 100 mL
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)	0.26 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	29.02 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73708-684-18	118.29 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/24/2020	08/23/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/24/2020	08/23/2022

Labeler - Carrollclean LLC (081222623)

Establishment
Name	Address	ID/FEI	Business Operations
Carrollclean		081222623	manufacture(73708-684)

Revised: 8/2020

Document Id: ad8fc24b-b6c9-7a05-e053-2a95a90aeb38

34390-5

Set id: ac3c4f2a-af88-7dd3-e053-2a95a90af769

Version: 2

Effective Time: 20200824