MICRODOT HAND SANITIZING WIPE- isopropyl alcohol liquid

microdot Hand Sanitizing Wipe by

Drug Labeling and Warnings

microdot Hand Sanitizing Wipe by is a Otc medication manufactured, distributed, or labeled by Cambridge Sensors USA, LLC, Guardsman Global. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Antiseptic Hand Sanitizing Wipe

ACTIVE INGREDIENT

Ethyl Alcohol 70.0 (w / w)

INDICATIONS & USAGE

Hand sanitizer to decrease bacteria on the skin.
For use when soap and water are not available.
Recommended for repeated use.

WARNINGS

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

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

WHEN USING

If irritation or rash appears, discontinue use. Consult a doctor if a condition persists longer than 72 hours.
If swallowed, get medical help or contact a Poision Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children unless under adult supervision.

DOSAGE & ADMINISTRATION

To open, remove lid and peal back seal. From center of roll of towels, pull up wipe corner, tear off first wipe and discard. Twist next wipe into a point and trhead through the hole in the container cover. Pull through about one inch. Replace cover.
Pull out wipes as needed and snap off at a 90° angle.

Using 1 wipe, take care to completely wet the full hand, then thoroughly wipe the hand, fingers, wrist, interdigital spaces and under the fingernails for 1 minute.
For visibly soiled hands, use first wipe to clean hands, then sanitize with a second wipe.

Keep cap closed to prevent evaporation.
Discard wipe after single use. DO NOT FLUSH.

OTHER SAFETY INFORMATION

Store at room temperature.

Lot Number and Expiration date can be found on the canister.

INACTIVE INGREDIENT

Aloe Barbadensis Leaf Juice, Purified water and Tocopheryl Acetate (Vitamin E).

PRINCIPAL DISPLAY PANEL

Product Label Image.

INGREDIENTS AND APPEARANCE

MICRODOT HAND SANITIZING WIPE 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52422-622
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52422-622-06	563.91 mL in 1 CANISTER; Type 0: Not a Combination Product	05/14/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/01/2025

Labeler - Cambridge Sensors USA, LLC (962314360)

Registrant - Cambridge Sensors USA, LLC (962314360)

Establishment
Name	Address	ID/FEI	Business Operations
Guardsman Global		117616105	label(52422-622) , manufacture(52422-622) , pack(52422-622)