OTC Medication Information: Lucky Instant Hand Sanitizer Citrus Zest

LUCKY INSTANT HAND SANITIZER CITRUS ZEST- alcohol liquid
Delta Brands Inc

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.

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

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

Warnings

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

When using this product

avoid contact with the skin and mucous membranes. I case of eye contact, immediately flush eyes with water, call a doctor. Avoid contact with broken skin.

Discontinue use if irritation develops. If condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children

Children can only use this product with adult supervision. Do not drink. Not edible. In case of accidental ingestion seek professional assistance or Poison Control Center immediately.

Other information

Do not store above 105ºF. May discolor some fabrics. Harmful to wood finishes and plastics.

Directions

Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. Recommended for repeated use.

Deionized Water, Isopropyl Alcohol, Glycerin, Carbomer, Triethanolamine, Propylene Glycol, PEG-40 Hydrogenated Castor Oil, Fragrance, Alphatocopherol Acetate (Vitamin E), FDC Yellow 5

Package Label

LUCKY INSTANT HAND SANITIZER CITRUS ZEST ethyl alcohol liquid

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:20276-156 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (ALCOHOL) ALCOHOL 62 mL in 100 mL

Inactive Ingredients Ingredient Name Strength WATER ISOPROPYL ALCOHOL GLYCERIN TROLAMINE PROPYLENE GLYCOL POLYOXYL 40 HYDROGENATED CASTOR OIL ALPHA-TOCOPHEROL ACETATE FD&C YELLOW NO. 5

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:20276-156-60 60 mL in 1 BOTTLE, SPRAY None 2 NDC:20276-156-02 2 BOTTLE, SPRAY in 1 BLISTER PACK contains a BOTTLE, SPRAY (20276-156-60) 2 NDC:20276-156-60 60 mL in 1 BOTTLE, SPRAY This package is contained within the BLISTER PACK (20276-156-02) 3 NDC:20276-156-05 148 mL in 1 BOTTLE, PUMP None 4 NDC:20276-156-08 237 mL in 1 BOTTLE, PUMP None 5 NDC:20276-156-10 296 mL in 1 BOTTLE, PUMP None 6 NDC:20276-156-12 355 mL in 1 BOTTLE, PUMP None 7 NDC:20276-156-24 710 mL in 1 BOTTLE, PUMP None 8 NDC:20276-156-36 1065 mL in 1 BOTTLE, PUMP None 9 NDC:20276-156-40 1183 mL in 1 BOTTLE, PUMP None 10 NDC:20276-156-48 1420 mL in 1 BOTTLE, PUMP None 11 NDC:20276-156-64 1893 mL in 1 BOTTLE, PLASTIC None 12 NDC:20276-156-85 3785 mL in 1 BOTTLE, PLASTIC None

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/01/2010

Labeler — Delta Brands Inc (102672008)

Revised: 09/2019 Delta Brands Inc