FAREWELL COLLECTION- antiseptic hand soap soap

Farewell Collection by

Drug Labeling and Warnings

Farewell Collection by is a Otc medication manufactured, distributed, or labeled by Paveemol Company Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzalkonium chloride 0.1%

Purpose

Antiseptic

Use

To help reduce bacteria on hands.

Warnings

For external use only.

Do not use

• in 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 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.

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 1 800-222-1222

Directions

Apply on hands thoroughly, wash and rinse afterward.

Children under 6 years of age should be supervised when using this product.

Other information

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

Inactive ingredients

acrylates copolymer, aloe barbadensis leaf extract, chlorphenesin, cocamidopropyl betaine, disodium EDTA, glycerin, maltodextrin, panthenol, PEG-40 hydrogenated castor oil, phenoxyethanol, PPG-26-Buteth-26, purified water USP, sodium benzoate, sodium hydroxide, sodium lauryl sulfate, tocopheryl acetate

Package Label - Principal Display Panel

250 mL NDC: 81892-116-11

INGREDIENTS AND APPEARANCE

FAREWELL COLLECTION 
antiseptic hand soap soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81892-116
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CHLORPHENESIN (UNII: I670DAL4SZ)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
PANTHENOL (UNII: WV9CM0O67Z)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81892-116-11	250 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/23/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/20/2021

Labeler - Paveemol Company Limited (660079138)

Establishment
Name	Address	ID/FEI	Business Operations
Paveemol Company Limited		660079138	manufacture(81892-116)