ASPICARE- alcohol solution

AspiCare by

Drug Labeling and Warnings

AspiCare by is a Otc medication manufactured, distributed, or labeled by American Private Label Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70% v/v.

Purpose

Antiseptic

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 the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or rash appears or lasts

Keep out of reach of children.

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
• Children under 6 years of age should be supervised when using ASPHICARE Hand sanitizer

Storage

• Store below 110°F (43°C)
• May discolor certain fabrics or surfaces

Inactive ingredients

Water (Aqua), Acrylates Copolymer, Aloe Barbadensis Leaf Juice, Glycerin, Isosteareth-200 Linoleate, Fragrance Triethanolamine

Other Information

Hand sanitizers provide a convenient alternative when hand washing with plain soap and water is unavailable. The Centers for Disease Control
and Prevention advises that washing hands with plain soap and running water is one of the most important steps consumers can take to avoid getting sick and to prevent spreading infections to others. If soap and water are not available, the CDC recommends using an alcohol-based hand sanitizer. Hand sanitizers should not replace hand washing with soap and water. FDA conducts ongoing review of OTC antiseptic active ingredients to determine whether these ingredients are safe and effective for their intended uses.

Principal Display Panel

NDC: 70735-070-01

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

1 FL OZ (30 mL)

NDC: 70735-070-02

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

2 FL OZ (60 mL)

NDC: 70735-070-03

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

3 FL OZ (89 mL)

NDC: 70735-070-04

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

4 FL OZ (118 mL)

NDC: 70735-070-06

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

6 FL OZ (177 mL)

NDC: 70735-070-08

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

8 FL OZ (236 mL)

NDC: 70735-070-16

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

16 FL OZ (473 mL)

NDC: 70735-070-32

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

32 FL OZ (946 mL)

INGREDIENTS AND APPEARANCE

ASPICARE 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70735-070
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70735-070-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020
2	NDC: 70735-070-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020
3	NDC: 70735-070-03	89 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020
4	NDC: 70735-070-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020
5	NDC: 70735-070-06	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020
6	NDC: 70735-070-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020
7	NDC: 70735-070-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020
8	NDC: 70735-070-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/09/2020

Labeler - American Private Label Products (051667474)

Registrant - American Private Label Products (051667474)