DERMEDICINE - ADVANCED HAND SANITIZER- alcohol gel

Dermedicine - Advanced Hand Sanitizer by

Drug Labeling and Warnings

Dermedicine - Advanced Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Cosmetic Solutions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

DRUG FACTS:

ACTIVE INGREDIENTS

Ethyl Alcohol 71% v/v

Purpose

Antimicrobial

USES

Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

WARNINGS

• Flammable. Keep away from fire or flame.

• For external use only.

• When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

• Stop use and seek a doctor if redness or irritation develops and persists for more than 72 hours.

Keep out of reach of children. Children under 6 years of age should be supervised when using this product.

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

DIRECTIONS

Put enough product in your palm to cover hands and rub hands together briskly until dry.

INACTIVE INGREDIENTS

Water (Aqua), Glycerin, Propanediol, Sodium Hyaluronate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylic/Capric Triglyceride, Tocopherol, Carthamus Tinctorius Oleosomes, Triethanolamine, Phenoxyethanol, Ethylhexylglycerin, Fragrance.

OTHER INFORMATION

Store at 68ºF to 77ºF (20ºC to 25ºC). May discolor fabrics.

SPL UNCLASSIFIED SECTION

Distributed by Cosmesis Skincare, Inc.
Hollywood, FL 33021

PRINCIPAL DISPLAY PANEL - 240 mL Bottle Label

dermedicine+
ADVANCED SKIN CARE

advanced
HAND
SANITIZER
gel

+
PROTECT &
MOISTURIZE

8 Fl. Oz. | 240mL

INGREDIENTS AND APPEARANCE

DERMEDICINE - ADVANCED HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66163-1503
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPANEDIOL (UNII: 5965N8W85T)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
TOCOPHEROL (UNII: R0ZB2556P8)
CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
TROLAMINE (UNII: 9O3K93S3TK)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66163-1503-1	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
2	NDC: 66163-1503-3	12 in 1 PACKAGE	04/01/2020
2	NDC: 66163-1503-1	120 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 66163-1503-2	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
4	NDC: 66163-1503-4	4 in 1 PACKAGE	04/01/2020
4	NDC: 66163-1503-2	240 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	04/01/2020

Labeler - Cosmetic Solutions LLC (807907928)