LUCKY HAND SANITIZER LAVENDER- ethyl 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.

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Hand Sanitizer Lavender 70

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

caprylyl glycol, carbomer, DC red no.33, FDC blue no.1, fragrance, glycerin, isopropyl alcohol, isopropyl myristate, PEG-40 hydrogenated castor oil, phenoxyehanol, propylene glycol, triethanolamine, tocopheryl acetate, water

image description

LUCKY HAND SANITIZER LAVENDER
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:20276-053
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
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)
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:20276-053-08	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/30/2012
2	NDC:20276-053-10	295 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/30/2012
3	NDC:20276-053-12	355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/30/2012

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

Labeler - Delta Brands Inc. (102672008)

Revised: 6/2023

Document Id: feba5de7-f4ca-2863-e053-6394a90a59ae

Set id: 7619c839-f8a2-4de5-b1ce-8b46424e674d

Version: 5

Effective Time: 20230622

Delta Brands Inc.