MOISTURISING HAND SANITIZER- alcohol gel

Moisturising Hand Sanitizer by

Drug Labeling and Warnings

Moisturising Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Oceanic SA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 71% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

• Hand Sanitizer to help reduce bacteria that potentially can cause disease.
• Recommended for repeated, frequent use.

Warnings

For external use only. Flammable. Keep away from fire or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

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. If swallowed, get medical help or contact a Poison Control Center right away.

STOP USE

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

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

• Place enough product in your palm to thoroughly cover your hands.
• Rub hands together until dry.
• Children under 6 years of age should be supervised when using this product.

Other information

• Store at the temperature below 110F (43C)
• May discolor certain fabrics or surfaces

Inactive ingredients

purified water USP, acrylates/c10-30 alkyl acrylates crosspolymer, glycerin, hyaluronic acid, triethanolamine, phenoxyethanol, ethylhexylglycerin, fragrance

Package Label - Principal Display Panel

Rescue Me by Rescue Spa

Mositurising Hand Sanitizer

Sachet 50 x 0.07 fl. oz. (50 x 2 mL)

Rescue Me by Rescue Spa

Mositurising Hand Sanitizer

1.69 fl.oz. / 50 mL

INGREDIENTS AND APPEARANCE

MOISTURISING HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79408-7001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HYALURONIC ACID (UNII: S270N0TRQY)	0.001 mL  in 100 mL
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.0009 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.2 mL  in 100 mL
TROLAMINE (UNII: 9O3K93S3TK)	0.2 mL  in 100 mL
WATER (UNII: 059QF0KO0R)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	0.0001 mL  in 100 mL
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)	0.8 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79408-7001-0	2 mL in 1 POUCH; Type 0: Not a Combination Product	07/24/2020
2	NDC: 79408-7001-2	1 in 1 CARTON	07/22/2020
2		50 mL in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 79408-7001-3	50 in 1 CARTON	07/22/2020
3		2 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/22/2020

Labeler - Oceanic SA (422218763)