Dr. Piercing Aftercare

Manufacturer: Broadway Products LLC
Effective date: 2023-07-29
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 21:27:52

Label at a glance#

ProductDr. Piercing Aftercare

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.11%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

FDA Registered antiseptic for the care and cleaning of piercings.

WARNINGS:

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions:

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aftercare Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81926-001-36	2024-01-30	C162847	48780-1	1030e365-510b-111a-e063-dadaa90a10e2	BROADWAY PRODUCTS (as PLD) - Dr. Piercing - Aftercare Swab (81926-001)

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

Dr. Piercing Aftercare
Benzalkonium Chloride
METHYLCHLOROISOTHIAZOLINONE
MAGNESIUM CHLORIDE
PANTHENOL
METHYLISOTHIAZOLINONE
MAGNESIUM NITRATE
CUPRIC NITRATE
WATER
COCAMIDOPROPYL BETAINE
TROLAMINE
SODIUM CHLORIDE
ALLANTOIN
ALOE VERA LEAF
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81926-001	81926-001-36

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
MAGNESIUM CHLORIDE	02F3473H9O	IACT
PANTHENOL	WV9CM0O67Z	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
MAGNESIUM NITRATE	77CBG3UN78	IACT
CUPRIC NITRATE	9TC879S2ZV	IACT
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
TROLAMINE	9O3K93S3TK	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
ALLANTOIN	344S277G0Z	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
29a41cf7-8739-6468-e063-6394a90a962e			c2a01d47-f887-57c8-e053-2a95a90aace1	2024-12-19	Warnings	Exact identifier spl set id: c2a01d47-f887-57c8-e053-2a95a90aace1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.