OTC Medication Information: Lucky Instant Hand Sanitizer with Vitamin E

LUCKY INSTANT HAND SANITIZER WITH VITAMIN E- 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 eyes and mucous membranes. In 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 mor 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 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),DC Red 33, FDC Blue 1

Package Label


image of package label

LUCKY INSTANT HAND SANITIZER WITH VITAMIN E
ethyl alcohol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:20276-152
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
D&C RED NO. 33
FD&C BLUE NO. 1
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:20276-152-60 60 mL in 1 BOTTLE, SPRAY None
2 NDC:20276-152-02 2 BOTTLE, SPRAY in 1 BLISTER PACK contains a BOTTLE, SPRAY (20276-152-60)
2 NDC:20276-152-60 60 mL in 1 BOTTLE, SPRAY This package is contained within the BLISTER PACK (20276-152-02)
3 NDC:20276-152-05 148 mL in 1 BOTTLE, PUMP None
4 NDC:20276-152-08 237 mL in 1 BOTTLE, PUMP None
5 NDC:20276-152-10 296 mL in 1 BOTTLE, PUMP None
6 NDC:20276-152-12 355 mL in 1 BOTTLE, PUMP None
7 NDC:20276-152-24 710 mL in 1 BOTTLE, PUMP None
8 NDC:20276-152-36 1065 mL in 1 BOTTLE, PUMP None
9 NDC:20276-152-40 1183 mL in 1 BOTTLE, PUMP None
10 NDC:20276-152-48 1420 mL in 1 BOTTLE, PUMP None
11 NDC:20276-152-64 1893 mL in 1 BOTTLE, PLASTIC None
12 NDC:20276-152-85 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

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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