FDA.reportPublic FDA data

DIPPIN DOTS ALCOHOL FREE HAND SANITIZER

Manufacturer
Flex Beauty Labs
Effective date
2020-08-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:23:49

Label at a glance#

ProductDIPPIN DOTS ALCOHOL FREE HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Dosage and administration

apply palmful to hands. rub hands together vigorously until dry. supervise children in the use of this product.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%.........Antibacterial

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin and clean hands.

Recommended for repeated uses.

Safety Instructions

WARNINGS SECTION

For extemal use only.

Do not Eat Or Drink

Flammable.Keep away from fire and flame.

When using this product

OTC - WHEN USING SECTION

In case of contact,rinse eyes thoroughly with water.

Do not use

OTC - DO NOT USE SECTION

Do  not use in or near eyes.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If accidentally swallowed, seek medical help or contact Poison Control  center right away.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), Polysorbate-20, PEG-40 Hydrogenated,Triethanolamine, Carbomer, Fragrance, Glycerin. Propylene Glycol, Calcium Sodium Borosilicate , Titanium Dioxide , Aloe Barbdensis Leaf Juice,Tocopheryl Acetate, Methylchloroisothiazolinone,Methylsothiazolinone ,Blue 1

Yellow 5,Red 9.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply palmful to hands.
  • rub hands together vigorously until dry.
  • supervise children in the use of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

dippin2dippin2

22

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1098199benzalkonium chloride 0.13 % Topical GelPSN2
1098199benzalkonium chloride 0.0013 MG/MG Topical GelSCD2
1098199benzalkonium chloride 0.13 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72308-026-792021-07-23C16284748780-1c7ccaba7-1c89-fd44-e053-dadaa90aa01bDIPPIN DOTS ALCOHOL FREE HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72308-026-79DIPPIN DOTS ALCOHOL FREE HAND SANITIZER2 in 1 PACKAGEGEL22
72308-026-79DIPPIN DOTS ALCOHOL FREE HAND SANITIZER79 mL in 1 BOTTLEGEL792

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72308-026DIPPIN DOTS ALCOHOL FREE HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [FLEX BEAUTY LABS]2Legacy NDC, 2 package rows20200805_bc3be834-77d8-4861-b673-bc760a1e36e4.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72308-02672308-026-79

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
POLYSORBATE 207T1F30V5YHIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
TROLAMINE9O3K93S3TKIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
ac0d4e25-3bd3-7131-e053-2a95a90aecacbc3be834-77d8-4861-b673-bc760a1e36e42020-08-04WarningsExact identifier
spl id: ac0d4e25-3bd3-7131-e053-2a95a90aecac
spl set id: bc3be834-77d8-4861-b673-bc760a1e36e4

Reported adverse events (FAERS/openFDA)#

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