BABYLISS PRO PROTECT HAND SANITIZER

Manufacturer
Conair Corporation
Effective date
2020-10-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:19

Label at a glance#

ProductBABYLISS PRO PROTECT HAND SANITIZER
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Apply. Put enough product on hands to cover all surfaces. Rub hands together, until hands feel dry. This should take around 20 seconds. Recommended for repeated use. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% V/V

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Antibacterial hand sanitizing gel to help kill bacteria and germs as antiseptic on the skin. For use when soap and water are not available.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only

When using this product

OTC - WHEN USING SECTION

keep out of eyes and mouth. In case of contact with eyes, immediately rinse eyes thoroughly with water.

Stop use and ask doctor if

OTC - STOP USE SECTION

irritation, rash or allergy occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply. Put enough product on hands to cover all surfaces. Rub hands together, until hands feel dry. This should take around 20 seconds. Recommended for repeated use. Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized Water. Carbomer. Panthenol. DMDM Hydantoin. Disodium EDTA. Triethanolamine.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
12829-0002-02022-01-28C16284748780-1d6a99b39-fe44-a426-e053-dadaa90af4c2BABYLISS PRO PROTECT HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12829-0002-0BABYLISS PRO PROTECT HAND SANITIZER12 in 1 BOXGEL121
12829-0002-0BABYLISS PRO PROTECT HAND SANITIZER488 mL in 1 BOTTLEGEL4881

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12829-0002BABYLISS PRO PROTECT HAND SANITIZER (ALCOHOL) GEL [CONAIR CORPORATION]1Legacy NDC, 2 package rows20201023_b2450142-e2c6-1abb-e053-2a95a90af172.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12829-000212829-0002-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
b244eb87-9297-9d40-e053-2995a90a5ae6b2450142-e2c6-1abb-e053-2a95a90af1722020-10-22WarningsExact identifier
spl id: b244eb87-9297-9d40-e053-2995a90a5ae6
spl set id: b2450142-e2c6-1abb-e053-2a95a90af172

Reported adverse events (FAERS/openFDA)#

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