GOOD DAY HAND SANITIZER- alcohol gel

GOOD DAY HAND SANITIZER by

Drug Labeling and Warnings

GOOD DAY HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Twila True Collaborations, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 70% v/v

Purpose

Antiseptic

Uses

• Hand sanitizer to help reduce bacteria on the skin.
• Recommended for repeated use.

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. If irritation persists, get medical advice.

Stop use and ask a doctor if

irritation develops or rash appears and lasts.

Keep out of reach of children.

Do not inhale or ingest. 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.
• For children under 6, use only under adult supervision. Not recommended for infants.

Other information

• Store below 110F (43C).
• May discolor some fabrics. Harmful to wood finishes and plastics. Questions? Send to: Twila True Collaborations, LLC 27156 Burbank, Foothill Ranch, CA 92610

Inactive ingredients

Water, Glycerin, Carbomer, Aminomethyl Propanol

Company Information

DISTRIBUTED BY TWILA TRUE COLLABORATIONS, LLC

FOOTHILL RANCH, CA 92610

WWW.GETGOODDAY.COM

FILLED IN THE U.S.A., MADE FROM LOCAL AND IMPORTED INGREDIENTS

Product Packaging - 946 mL

​GOOD DAY

FILLED IN THE U.S.A.

hand

sanitizer

CLEAN + FRESH GEL FORMULA

alcohol antiseptic 70%

topical solution

non-sterile solution

32 FL OZ/946 mL

INGREDIENTS AND APPEARANCE

GOOD DAY HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75070-070
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75070-070-12	354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/29/2020
2	NDC: 75070-070-08	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/29/2020
3	NDC: 75070-070-32	946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/29/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/29/2020

Labeler - Twila True Collaborations, LLC (117034809)