SENTINEL HAND SANITIZER- alcohol spray

SENTINEL HAND SANITIZER by

Drug Labeling and Warnings

SENTINEL HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by DANLAB DANUTA KATRYNSKA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75% v/v.

Purpose

Antiseptic

Use

• To decrease bacteria on the skin that coucld cause disease.
• Recommended for repeated use.

Warnings

For external use only:hands.

Flammable. Keep away from heat or flame.

When using this product

• keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• Avoid contact with broken skin.
• Do not inhale or ingest.
• Stop use and ask a doctor if
• irritation or redness develops.
• Condition persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Wet hands thoroughly with product and allow to dry without wiping.
• For children under 6, use only under adult supervision.
• Not recommended for infants.

Other information

• Do not store above 1050F
• May discolor certain fabrics.
• Harmful to wood finishes and plastics

Inactive ingredients

Water (Aqua), Isopropyl alcohol, Plant pharma glycerin, Peppermint oil.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

SENTINEL HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79041-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
PEPPERMINT OIL (UNII: AV092KU4JH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79041-002-01	59 mL in 1 TUBE; Type 0: Not a Combination Product	06/18/2020
2	NDC: 79041-002-02	75 mL in 1 TUBE; Type 0: Not a Combination Product	06/18/2020
3	NDC: 79041-002-03	118 mL in 1 TUBE; Type 0: Not a Combination Product	06/18/2020
4	NDC: 79041-002-04	125 mL in 1 TUBE; Type 0: Not a Combination Product	06/18/2020
5	NDC: 79041-002-05	236 mL in 1 TUBE; Type 0: Not a Combination Product	06/18/2020
6	NDC: 79041-002-06	250 mL in 1 TUBE; Type 0: Not a Combination Product	06/18/2020
7	NDC: 79041-002-07	500 mL in 1 TUBE; Type 0: Not a Combination Product	06/18/2020
8	NDC: 79041-002-08	1000 mL in 1 TUBE; Type 0: Not a Combination Product	06/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/18/2020

Labeler - DANLAB DANUTA KATRYNSKA (422359029)