Natural Care Advanced Hand Sanitizer, Alcohol Antiseptic 62%

Natural Care Advanced Hand Sanitizer, Alcohol Antiseptic 62 by

Drug Labeling and Warnings

Natural Care Advanced Hand Sanitizer, Alcohol Antiseptic 62 by is a Otc medication manufactured, distributed, or labeled by Dr. Natural LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NATURAL CARE ADVANCED HAND SANITIZER, ALCOHOL ANTISEPTIC 62- alcohol gel 
Dr. Natural LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Natural Care Advanced Hand Sanitizer, Alcohol Antiseptic 62%

Drug Facts

Active Ingredients

Ethyl Alcohol 62% 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:

NATURAL CARE ADVANCED HAND SANITIZER, ALCOHOL ANTISEPTIC 62 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78261-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 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: 78261-001-05	155.3 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)

Revised: 7/2020

Document Id: abc2a727-64cb-c644-e053-2995a90ab17a

34390-5

Set id: abc2a727-64ca-c644-e053-2995a90ab17a

Version: 1

Effective Time: 20200731