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 gel 
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 fire or flame.

When using this product avoid contact with eyes. If eye contact occurs, rinse with water.

Stop use and ask a doctor if irritation or redness develops.

Keep out of reach of children. In case of accidental ingestion, seek medical help or contact poison control center right away.

Uses

• To help reduce bacteria on the skin.

Directions

• Apply enough gel to wet hands and rub together until dry.
• Use 1 to 3 times daily.

Other information

• Do not store above 104°F/40°C

Inactive ingredients Water (Aqua), Isopropyl Alcohol, Hydroxyethylcellulose, Glycerin, Salvia Hispanica (Chia) Seed Oil, Helianthus Annuus (Sunflower) Seed Oil, Rosmarinus Officinalis (Rosemary) Leaf Extract and Fragrance (Parfum)

SENEGENCE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72644-629
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
SALVIA HISPANICA SEED (UNII: NU0OLX06F8)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
GLYCERIN (UNII: PDC6A3C0OX)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ROSEMARY (UNII: IJ67X351P9)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72644-629-05	14 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020	06/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/06/2020	06/01/2021

Labeler - SGII, Inc (070096792)

Revised: 12/2021

Document Id: d2aff5d1-b722-334d-e053-2a95a90a42b1

34390-5

Set id: ac3f9f14-1eb4-fa6e-e053-2a95a90aa17c

Version: 2

Effective Time: 20211208