FDA.reportPublic FDA data

Beautyfrizz Hand Sanitizer Lotion bzk Hemp

Manufacturer
BBC GROUP LIMITED
Effective date
2020-05-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:28

Label at a glance#

ProductHand Sanitizer Alcohol Free with Hemp Oil Shea Butter
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

■ Hand sanitizing lotion to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

■ Apply a dime-sized amount onto hands and rub together until absorbed. ■ Supervise children under 6 years of age when using this product

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ Hand sanitizing lotion to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

■ keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes throughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develops and persists.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, contact a doctor or Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Apply a dime-sized amount onto hands and rub together until absorbed. ■ Supervise children under 6 years of age when using this product

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Mineral Oil, Cetearyl Alcohol, Glycerin, Glyceryl Stearate, Steareth-25, PEG-100 Stearate, Urea, Dimethicone, Shea (Butyrospermum Parkii) Butter, Phenoxyethanol, Xanthan Gum, Hemp (Cannabis) Seed Oil, Chlorphenesin, Sodium Hyaluronate

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046442benzalkonium chloride 0.13 % Topical LotionPSN1
1046442benzalkonium chloride 1.3 MG/ML Topical LotionSCD1
1046442benzalkonium chloride 0.13 % Topical LotionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76383-031-032022-01-28C16284748780-1d6a99b39-c12f-a426-e053-dadaa90af4c2Beautyfrizz Hand Sanitizer Lotion bzk Hemp

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76383-031-03Hand SanitizerAlcohol Free with Hemp Oil Shea Butter100 mL in 1 TUBELOTION1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76383-031HAND SANITIZER ALCOHOL FREE WITH HEMP OIL SHEA BUTTER (BENZALKONIUM CHLORIDE) LOTION [BBC GROUP LIMITED]1Legacy NDC, 1 package rows20200524_a658c63f-a9ff-4d1d-e053-2995a90afd46.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76383-03176383-031-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONATE SODIUMYSE9PPT4THIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
CHLORPHENESINI670DAL4SZIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
STEARETH-2536ALR4705BIACT
PEG-100 STEARATEYD01N1999RIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
UREA8W8T17847WIACT
DIMETHICONE92RU3N3Y1OIACT
SHEA BUTTERK49155WL9YIACT
PHENOXYETHANOLHIE492ZZ3TIACT
XANTHAN GUMTTV12P4NEEIACT
MINERAL OILT5L8T28FGPIACT

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
a6589353-6f9a-8ba8-e053-2995a90a7e78a658c63f-a9ff-4d1d-e053-2995a90afd462020-05-23WarningsExact identifier
spl id: a6589353-6f9a-8ba8-e053-2995a90a7e78
spl set id: a658c63f-a9ff-4d1d-e053-2995a90afd46

Reported adverse events (FAERS/openFDA)#

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