Warner Friends Sanitizer Clip and Clean OH MY GOD Peach

Manufacturer
Mad Beauty USA LLC
Effective date
2021-12-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:23:37

Label at a glance#

ProductWarner Friends Sanitizer Clip and Clean OH MY GOD Peach
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Reduce bacteria on hands.

Dosage and administration

Place pea sized drop onto hands. Supervise children under 6 years of age when using this produt to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 69%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Reduce bacteria on hands.

Warnings

WARNINGS SECTION

Flammable. Keep away from source of Ignition or flame.  

For external use only.

Do not use

OTC - DO NOT USE SECTION

on open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a doctor immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place pea sized drop onto hands.
  • Supervise children under 6 years of age when using this produt to avoid swallowing.

Other Information

SPL UNCLASSIFIED SECTION

Store between 15-30°C (59-86°F). Avoid freezing and excessive heat above 40°C (104°F).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua,Eau), Pentylene Glycol, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Butylene Glycol, Fragrance(Parfum), Sodium Hydroxide, Aloe Barbadensis (Aloe Vera)Leaf Extract, CI 19140(FD&C Yellow 5).

Questions or Comments

OTC - QUESTIONS SECTION

MAD BEAUTY USA LLC

1030 SALEM ROAD

UNION NJ 07083 

TEL (844) 995 1701

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabel2Label2

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78789-04378789-043-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
d2bd7382-2b7c-6448-e053-2a95a90aa578ae6e0101-eb06-65ee-e053-2a95a90a698d2021-12-09WarningsExact identifier
spl id: d2bd7382-2b7c-6448-e053-2a95a90aa578
spl set id: ae6e0101-eb06-65ee-e053-2a95a90a698d

Reported adverse events (FAERS/openFDA)#

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