Secrete plus wipes

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co.,Ltd
Effective date
2022-12-03
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:43:46

Label at a glance#

ProductSecrete plus wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Wipe hands thoroughly with towelette. Allow to dry. Discard after single use. For occasional and personal domestic use. Do not flush. Children should be supervised by an adult when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% w/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial   

Use

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin that may cause disease.

Warnings

WARNINGS SECTION

For external use only.
When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if irritation occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

Wipe hands thoroughly with towelette. Allow to dry. Discard after single use. For occasional and personal domestic use.
Do not flush. Children should be supervised by an adult when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Fragrance (Parfum), Tocopheryl Acetate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80204-050-012022-03-07C16284748780-1d6a99b39-7c4a-a426-e053-dadaa90af4c245505f0d-b1e4-4a76-a198-dce9a423389d
80204-050-012022-01-28C16284748780-1d6a99b39-7c4a-a426-e053-dadaa90af4c245505f0d-b1e4-4a76-a198-dce9a423389d

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80204-05080204-050-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
244b9b58-8c8d-43a3-b4b1-dc8c21fe56f945505f0d-b1e4-4a76-a198-dce9a423389d2022-12-03WarningsExact identifier
spl id: 244b9b58-8c8d-43a3-b4b1-dc8c21fe56f9
spl set id: 45505f0d-b1e4-4a76-a198-dce9a423389d

Reported adverse events (FAERS/openFDA)#

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