ADAMS POLISHES HAND SANITIZER- isopropyl alcohol solution

ADAMS POLISHES HAND SANITIZER by

Drug Labeling and Warnings

ADAMS POLISHES HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Crystal Packaging, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Isopropyl Alcohol 75% v/v

Purpose

Antiseptic

Use[s]

Hand rub to help reduce bacteria that potentially can cause disease.

Warnings

For external use only.

Flammable. Keep away from heat or flame.

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP.

Questions or Comments?

Call 1-866-965-0400

Monday through Friday 8:00AM to 5:00PM MST.

SPL UNCLASSIFIED SECTION

  TOPICAL SOLUTION

ANTISEPTIC HAND RUB  NON-STERILE SOLUTION

FAST ACTING ANTISEPTIC UNSCENTED AND LEAVES HANDS SOFT AND SMOOTH

FORMULATED IN ACCORDANCE WITH World Health Organization RECOMMENDATIONS

MANUFACTURED AND BOTTLED IN AN FDA REGISTERED FACILITY IN THE U.S.A

AdamsPolishes.com

Manufactured by

B&B Blending, LLC, Northglenn, CO USA

www.bbblending.com

Packaging

INGREDIENTS AND APPEARANCE

ADAMS POLISHES HAND SANITIZER 
isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74508-170
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74508-170-80	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/27/2020

Labeler - Crystal Packaging, Inc. (160837019)

Establishment
Name	Address	ID/FEI	Business Operations
Crystal Packaging, Inc.		160837019	manufacture(74508-170)