73792-0004_Kiss Hand Sanitizer Spray

Kiss Hand Sanitizer by

Drug Labeling and Warnings

Kiss Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SAE HAN COSMETICS LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KISS HAND SANITIZER- alcohol spray 
SAE HAN COSMETICS LTD

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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73792-0004_Kiss Hand Sanitizer Spray

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antiseptic

Use

• Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

Flammable. Keep away from fire or flame.

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts

Keep out of reach of children.

Other information

• Store betweem 15-30°C (59-86°F)
• Avoid freezing and excessive heat above 40°C (104°F)

Directions

Spray directly on hands and rub thoroughly until dry.

Inactive ingredients

Water, Glycerin, Lavandula Angustifolia (Lavender) Flower Extract, Monarda Didyma Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Freesia Refracta Extract, Chamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Butylene Glycol, 1,2-Hexanediol, Ethylhexylglycerin, Aloe Barbadensis Leaf Juice Powder, Maltodextrin, Fragrance

KISS HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73792-0004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
MONARDA DIDYMA LEAF (UNII: JY15982UBB)
MENTHA PIPERITA LEAF (UNII: A389O33LX6)
FREESIA ALBA WHOLE (UNII: SS55L6C3QQ)
CHAMOMILE (UNII: FGL3685T2X)
ROSEMARY (UNII: IJ67X351P9)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MALTODEXTRIN (UNII: 7CVR7L4A2D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73792-0004-1	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/17/2020	12/06/2021
2	NDC: 73792-0004-2	250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/17/2020	12/06/2021
3	NDC: 73792-0004-3	295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/17/2020	12/06/2021
4	NDC: 73792-0004-4	325 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/17/2020	12/06/2021
5	NDC: 73792-0004-5	355 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/17/2020	12/06/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/17/2020	12/06/2021

Labeler - SAE HAN COSMETICS LTD (687835025)

Registrant - SAE HAN COSMETICS LTD (687835025)

Establishment
Name	Address	ID/FEI	Business Operations
SAE HAN COSMETICS LTD		687835025	manufacture(73792-0004)

Revised: 12/2021

Document Id: d2857d9d-42dc-ccf1-e053-2995a90a9fab

34390-5

Set id: dd2559a7-5368-469f-b564-1e41891d608f

Version: 2

Effective Time: 20211206