Lucky Instant Hand Cleanser with Aloe Vera

Dosage form: liquid
Ingredients: ALCOHOL 62mL in 100mL
Labeler: Delta Brands Inc
NDC Code: 20276-157

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.

Drug Facts

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

UsesHand 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 productavoid contact with eyes an 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 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 InformationDo not store above 105F. May discolor some fabrics. Harmful to wood finishes and plastics

DirectionsPlace 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)

Package Label

LUCKY INSTANT HAND CLEANSER WITH ALOE VERA 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-157
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ISOPROPYL ALCOHOL 
GLYCERIN 
TROLAMINE 
PROPYLENE GLYCOL 
POLYOXYL 40 HYDROGENATED CASTOR OIL 
ALOE VERA LEAF 
FD&C YELLOW NO. 5 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:20276-157-6060 mL in 1 BOTTLE, PLASTIC
2NDC:20276-157-022 BOTTLE, PLASTIC (BOTTLE) in 1 BLISTER PACK
2NDC:20276-157-6060 mL in 1 BOTTLE, PLASTIC
3NDC:20276-157-033 BOTTLE, PLASTIC (BOTTLE) in 1 BLISTER PACK
3NDC:20276-157-6060 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33312/08/2009
Labeler - Delta Brands Inc (102672008)
Establishment
NameAddressID/FEIOperations
Ningbo Pulisi Daily Chemical Co. Ltd.529047265manufacture

Revised: 12/2009
 
Delta Brands Inc

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide
(web3)