LUCYS RENEWALS SKIN AND NAILS FIRST AID ANTISEPTIC- benzethonium chloride solution

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active ingredients

Benzethonium Chloride 0.20%

Purpose

First Aid Antiseptic

Uses

• First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

Warnings

For external use only.

Do not use

on children less than 3 years of age
on open skin wounds in the eyes or apply over large areas of the body
in case of deep or puncture wounds, animal bites, or serious burns, consult a doctor
longer than 1 week unless directed by a doctor.

When using this product

•  keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Children under 6 years of age must be supervised when using this product.

Stop use and ask a doctor if

the condition persists or gets worse, or if a rash or other allergic reaction develops.
Allergy alert  Do not use if you are allergic to any of the ingredients.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding,

ask a health professional before use.

Directions:

Shake well.  Apply product on clean dry skin or nails 1-3 times daily.  When applied on nails cover the whole nail zone including under the nail, let it dry.  Remove with plenty of water or isopropyl.  Product can be applied over nail polish.

Other information:

Do not expose to excessive heat.
Store at room temperature 68°F to 77°F (20° to 25°C)

Inactive ingredients:

Acetic Acid, Acetyl Tributyl Citrate, Adipic Acid/Neopentyl Glycol/Trimellitic Anhydride Copolymer, Alcohol, Benzophenone-3, Butyl Acetate, Ethoxyethane, Ethyl Acetate, Isopropyl Alcohol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Nitrocellulose, Trimethylpentanediyl Dibenzoate, Violet 2 (CI 60725), Water (Aqua).

Package Labeling:

INGREDIENTS AND APPEARANCE

LUCYS RENEWALS SKIN AND NAILS FIRST AID ANTISEPTIC 
benzethonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87672-961
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	2 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ACETIC ACID (UNII: Q40Q9N063P)
ACETYL TRIBUTYL CITRATE (UNII: 0ZBX0N59RZ)
ADIPIC ACID (UNII: 76A0JE0FKJ)
NEOPENTYL GLYCOL (UNII: QI80HXD6S5)
ALCOHOL (UNII: 3K9958V90M)
OXYBENZONE (UNII: 95OOS7VE0Y)
BUTYL ACETATE (UNII: 464P5N1905)
ETHER (UNII: 0F5N573A2Y)
ETHYL ACETATE (UNII: 76845O8NMZ)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TEA TREE OIL (UNII: VIF565UC2G)
PYROXYLIN (UNII: KYR8BR2X6O)
TRIMETHYLPENTANEDIYL DIBENZOATE (UNII: Y8PB83G67A)
D&C VIOLET NO. 2 (UNII: 350KA7O6HK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87672-961-00	1 in 1 BOX	02/16/2026
1		30 mL in 1 BOTTLE; 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	02/16/2026

Labeler - ACP Laboratories LLC (041955491)

Registrant - Pure Source, LLC (080354456)