NATURAL CARE ADVANCED HAND SANITIZER, ALCOHOL ANTISEPTIC 70- alcohol gel

Natural Care Advanced Hand Sanitizer, Alcohol Antiseptic 70 by

Drug Labeling and Warnings

Natural Care Advanced Hand Sanitizer, Alcohol Antiseptic 70 by is a Otc medication manufactured, distributed, or labeled by Dr. Natural LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Ethyl Alcohol 70% w/w

Purpose

Antibacterial

Use

hand sanitizer to help reduce bacteria on the skin.

Warnings

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

When using this product

do not use in or near eyes. In case of contact,rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or redness develops.

Keep out of reach of children.

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

Directions

• apply palmful to hands
• rub hands together vigorously until dry
• supervise children in the use of this product.

Other information

• store below 110°F (43°C)
• may discolor certain fabrics or surfaces.

Inactive ingredients

Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Fragrance, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice (Aloe Vera), Tocopheryl Acetate(Vitamin E), Yellow 5 (CI 19140), Blue 1 (CI 42090).

Package Labeling:349ml

Package Labeling:946ml

INGREDIENTS AND APPEARANCE

NATURAL CARE ADVANCED HAND SANITIZER, ALCOHOL ANTISEPTIC 70 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78261-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78261-002-11	349 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
2	NDC: 78261-002-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2020

Labeler - Dr. Natural LLC (080454165)