LUCKY HAND SANITIZER WITH ALOE VERA- ethyl alcohol liquid

Lucky by

Drug Labeling and Warnings

Lucky by is a Otc medication manufactured, distributed, or labeled by Delta Brands Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70% v/v

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 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 should only use this product under adult supervision. Do not drink. Not edible. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Other information

do not store above 105F. 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

Inactive ingredients

aloe barbedensis leaf extract, caprylyl glycol, carbomer, FDC blue no. 1, FDC yellow no. 5, fragrance, glycerin, isopropyl alcohol, isopropyl myristate, PEG-40 hydrogenated castor oil, phenoxyehanol, propylene glycol, triethanolamine, water

Package Label

Package Label

INGREDIENTS AND APPEARANCE

LUCKY  HAND SANITIZER WITH ALOE VERA
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20276-052
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20276-052-08	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/30/2012
2	NDC: 20276-052-10	295 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/30/2012
3	NDC: 20276-052-12	355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/30/2012
4	NDC: 20276-052-02	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/30/2012

Labeler - Delta Brands Inc. (102672008)