SeneGence Hand Sanitizer by SGII, Inc SeneGence Hand Sanitizer

SeneGence Hand Sanitizer by

Drug Labeling and Warnings

SeneGence Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SGII, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SENEGENCE HAND SANITIZER- alcohol solution 
SGII, 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.

----------

SeneGence Hand Sanitizer

Active Ingredient

Alcohol 62% v/v

Purpose

Antiseptic

• For external use only.
• Flammable, Keep away from heat or flame.

When using this product keep out of eyes, ears and mouth. If case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses

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

Directions

• Place enough product on hands to cover all surfaces.
• Rub hands together until dry
• Supervise children under 6 years of age when using this product to avoid swallowing

Other information

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

Inactive ingredients Aloe Barbadensis Leaf Juice, Carthamus Tinctorius (Safflower) Oleosomes, Cymbopogon Flexuosus (Lemongrass) Oil, Fragrance (Parfum), Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Hydroxyethylcellulose, Lonicera Caprifolium (Honeysuckle) Flower Extract, Lonicera Japonica (Honeysuckle) Flower Extract, PEG-40 Hydrogenated Castor Oil, Rosmarinus Officinalis (Rosemary) Leaf Extract, Sodium Hyaluronate, Water (Aqua), Yellow 10 (CI 47005). May contain Isopropyl Alcohol.

SENEGENCE HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72644-628
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SAFFLOWER (UNII: 4VBL71TY4Y)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
GLYCERIN (UNII: PDC6A3C0OX)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ROSEMARY (UNII: IJ67X351P9)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
WATER (UNII: 059QF0KO0R)
CYMBOPOGON FLEXUOSUS WHOLE (UNII: 0MK18YOA5G)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72644-628-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020	05/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/07/2020	05/01/2021

Labeler - SGII, Inc (070096792)

Revised: 12/2021

Document Id: d2affc41-2805-95ff-e053-2995a90a648f

34390-5

Set id: a9e3b8c4-fe89-2869-e053-2a95a90a5654

Version: 2

Effective Time: 20211208