Activa by Lenaco Corporation dba Blue Ribbon Supply Company ACTIVA- alcohol cloth

Activa by

Drug Labeling and Warnings

Activa by is a Otc medication manufactured, distributed, or labeled by Lenaco Corporation dba Blue Ribbon Supply Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Uses

• For handwashing to decrease bacteria on skin.
• After changing diapers. After assisting ill persons.
• Before contact with a person under medical care or treatment.
• Recommended for repeated use.

Warnings

For external use only.
Flammable. Keep away from fire or flame.
When using this productavoid contact with eyes. If contact occurs. flush thoroughly with water.
Discontinue use and contact a doctor ifirritation and redness develop and conditions persist for more than 72 hours.

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.

Directions

Wet hands thoroughly with product for approximately 15 seconds and allow to dry. Children under six years of age should be supervised when using this product. Throw used wipe in trash. Do not flush.

Other information

Store below 104°F (40°C).

Inactive ingredients

Water, Propylene Glycol, Undeceth-7. lsopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E), and Fragrance

NFPA ®Ratings
Health:0; Flammability:3; Reactivity:0

Product label

INGREDIENTS AND APPEARANCE

ACTIVA 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80552-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
UNDECETH-7 (UNII: R6B5PCO2JN)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80552-001-01	10 in 1 PACKET	09/01/2020
1		4 mL in 1 CANISTER; Type 0: Not a Combination Product
2	NDC: 80552-001-02	100 in 1 CANISTER	09/01/2020
2		4 mL in 1 CANISTER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/01/2020

Labeler - Lenaco Corporation dba Blue Ribbon Supply Company (029162450)