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 70mL

Rescue Me by Rescue Spa

Mositurising Hand Sanitizer 250mL

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
4	NDC: 79408-7001-5	1 in 1 CARTON	07/22/2020
4		70 mL in 1 TUBE; Type 0: Not a Combination Product
5	NDC: 79408-7001-4	1 in 1 CARTON	07/22/2020
5		250 mL in 1 BOTTLE; 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)