APOLLO MEDICAL PRODUCTS DISINFECTING WIPES- alcohol liquid

Apollo Medical Products Disinfecting Wipes by

Drug Labeling and Warnings

Apollo Medical Products Disinfecting Wipes by is a Otc medication manufactured, distributed, or labeled by KKJ & Associates LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 70% v/v.

Purpose

Antiseptic

Use

For first aid and for cleansing areas to reduce bacteria and viruses.

Warnings

For external use only. Flammable. Keep away from heat or flame. Store at room temperature 59F-86F (15C-30C)

Do not use

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

WHEN USING

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

STOP USE

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. POISON CONTROL (800)-222-1222

Directions

Clean the affected area by using wipe to apply and clean skin or surface. Let air dry.

Other information

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

Inactive ingredients

Water.

STORAGE AND HANDLING

Dispose of wipe in trash after use. Do not flush. Tightly close lids between uses to retain moisture. Nonrefillable container. Do not reuse or refill this empty container. Offer empty containers for recycling. If recycling is not available, discard container in trash.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

APOLLO MEDICAL PRODUCTS DISINFECTING WIPES 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79642-003
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79642-003-01	1 in 1 CONTAINER	09/18/2020
1		500 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/18/2020

Labeler - KKJ & Associates LLC (057060784)

Establishment
Name	Address	ID/FEI	Business Operations
KKJ & Associates LLC		057060784	manufacture(79642-003)