ASPICARE- isopropyl rubbing 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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AspiCare Isopropyl Rubbing Alcohol

Active Ingredient

Isopropyl Alcohol 70% v/v.

Purpose

First Aid Antiseptic

Use

helps prevent the risk of infection in:

Warnings

For external use only.

Flammable • Keep away from fire or flame, heat, spark, or electrical

Ask a doctor before use

or deep or puncture wounds, animal bites or serious burns

When using this product

do not get into eyes • do not inhale • do not apply over large areas of the body • do not use longer than 1 week

Stop use and ask a doctor if

condition persists or gets worse

Keep out of reach of children

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

Caution

Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

Directions

Clean the affected area • apply a small amount of this product on the area 1 to 3 times daily • may be covered with a sterile bandage • if bandaged, let dry first

Storage

Inactive ingredients

Water (Aqua)

Other Information

Does not contain, nor is intended as a substitute for grain or ethyl alcohol • will produce serious gastric disturbances if taken internally.

Principal Display Panel

NDC 70735-072-08, 70735-072-16, 70735-072-32, 70735-072-28

Isopropyl Rubbing Alcohol 70%

FIRST AID ANTISEPTIC

WARNING FLAMMABLE

Keep away from heat, spark, electrical, fire or flame

Use only in a well-ventilated area; fumes may be harmful.

Caution: Do not point at self or others; Product will squirt when squeezed.

8 FL OZ (236 mL)

16 FL OZ (473 mL)

32 FL OZ (946 mL) 1 Litre

128 FL OZ (3785 mL)

Label

ASPICARE 
isopropyl rubbing alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70735-072
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70735-072-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product03/08/2021
2NDC:70735-072-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product03/08/2021
3NDC:70735-072-32946 mL in 1 BOTTLE; Type 0: Not a Combination Product03/08/2021
4NDC:70735-072-283785 mL in 1 BOTTLE; Type 0: Not a Combination Product03/08/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/08/2021
Labeler - American Private Label Products (051667474)
Registrant - American Private Label Products (051667474)

Revised: 3/2021
Document Id: cbf1dbe7-aded-4184-88b8-cfae1e2100ae
Set id: 3f2afdff-0a73-4831-b874-b48cae1609be
Version: 1
Effective Time: 20210308
 
American Private Label Products