FAREWELL COLLECTION- antiseptic shower cream cream

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 0.05 %.

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 skin thoroughly, wash, and rinse. Suitable to daily use.
• Supervise children under 6 years of age when using this product to avoid swallowing.

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, glycol distearate, maltodextrin, phenoxyethanol, polyquaternium-7, propylene glycol, purified water USP, shea butter, sodium benzoate, sodium coco-sulfate, sodium laureth sulfate, triethanolamine.

Package Label - Principal Display Panel

250 mL NDC : 81892-115-11

INGREDIENTS AND APPEARANCE

FAREWELL COLLECTION 
antiseptic shower cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81892-115
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.05 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHLORPHENESIN (UNII: I670DAL4SZ)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
SODIUM COCO-SULFATE (UNII: 3599J29ANH)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SHEA BUTTER (UNII: K49155WL9Y)
MALTODEXTRIN (UNII: 7CVR7L4A2D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81892-115-11	250 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/22/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/22/2021

Labeler - Paveemol Company Limited (660079138)

Establishment
Name	Address	ID/FEI	Business Operations
Paveemol Company Limited		660079138	manufacture(81892-115)