ASPICARE- alcohol solution 
American Private Label Products

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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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

Storage

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)

Label 1

NDC 70735-070-02

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

2 FL OZ (60 mL)

Label 2

NDC 70735-070-03

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

3 FL OZ (89 mL)

Label 3

NDC 70735-070-04

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

4 FL OZ (118 mL)

Label 4

NDC 70735-070-06

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

6 FL OZ (177 mL)

Label 6

NDC 70735-070-08

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

8 FL OZ (236 mL)

Label 8

NDC 70735-070-16

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

16 FL OZ (473 mL)

Label 16

NDC 70735-070-32

AspiCare

HAND SANITIZER

KILLS 99% OF GERMS*

Moisturizer Leaves Hands Smooth

MADE IN USA

32 FL OZ (946 mL)

Label 32

ASPICARE 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70735-070
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70735-070-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2020
2NDC:70735-070-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2020
3NDC:70735-070-0389 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2020
4NDC:70735-070-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2020
5NDC:70735-070-06177 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2020
6NDC:70735-070-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2020
7NDC:70735-070-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2020
8NDC:70735-070-32946 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/09/2020
Labeler - American Private Label Products (051667474)
Registrant - American Private Label Products (051667474)

Revised: 4/2020
Document Id: 8bc3322b-7edd-4b0a-87dc-d06102ecd46a
Set id: 0db00216-446e-45d0-a7e8-24b8ec409333
Version: 1
Effective Time: 20200409
 
American Private Label Products