BROADWAY PRODUCTS (as PLD) - Dr. Piercing - Aftercare Swab (81926-001)

Dr. Piercing Aftercare by

Drug Labeling and Warnings

Dr. Piercing Aftercare by is a Otc medication manufactured, distributed, or labeled by Broadway Products LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DR. PIERCING AFTERCARE- benzalkonium chloride swab 
Broadway Products LLC

----------

BROADWAY PRODUCTS (as PLD) - Dr. Piercing - Aftercare Swab (81926-001)

ACTIVE INGREDIENTS

Benzalkonium Chloride 0.11%

Purpose

Antiseptic

Use

FDA Registered antiseptic for the care and cleaning of piercings.

WARNINGS:

For external use only.If redness, irritation, infection or swelling occurs, discontinue use and consult a physician. Keep out of eyes. Do not insert into the ear canal. Store at room temprature.

Keep out of reach of children.

Directions:

1. Hold swab with the colored round marker end up.

2. Bend the colored round marker tip until it "snaps".

3. Liquid flows down into the white tip.

4. Apply medicated tip to piercing. Dispose.

OTHER INGREDIENTS

Isotonic Saline Solution, Aloe Vera, Allantoin, Panthenol/Pro-Vitamin B5.

DR. PIERCING AFTERCARE 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81926-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
PANTHENOL (UNII: WV9CM0O67Z)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
CUPRIC NITRATE (UNII: 9TC879S2ZV)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
TROLAMINE (UNII: 9O3K93S3TK)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALLANTOIN (UNII: 344S277G0Z)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81926-001-36	36 in 1 CASE	01/01/2021	09/23/2024
1		0.15 mL in 1 APPLICATOR; 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	01/01/2021	09/23/2024

Labeler - Broadway Products LLC (002672936)

Revised: 12/2024

Document Id: 29a41cf7-8739-6468-e063-6394a90a962e

34390-5

Set id: c2a01d47-f887-57c8-e053-2a95a90aace1

Version: 7

Effective Time: 20241219