FDA.reportPublic FDA data

Personal CARE

Manufacturer
Delta Brands & Products LLC
Effective date
2018-04-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:00:14

Label at a glance#

ProductPersonal CARE Hand Sanitizer with Moisturizers Vitamin E
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

■ place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry ■ children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire and flame. For external use only

When using this product

OTC - WHEN USING SECTION

■ do not use i or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

■irritation or rash appears and lasts

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

■ place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry ■ children under 6 years of age should be supervised when using this product

Other infromation

SPL UNCLASSIFIED SECTION

■ store below 105ºF(41ºC) ■ may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, aloe barbadensis leaf juice,carbomer, fragrance, glycerin, propylene glycol, tocopheryl acetate (vitamin E), triethanolamine

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72133-051-022020-09-27C16284748780-1ab0e2407-323e-f274-e053-dbdaa90a6471Drug Facts
72133-051-082020-09-27C16284748780-1ab0e2407-323e-f274-e053-dbdaa90a6471Drug Facts
72133-051-122020-09-27C16284748780-1ab0e2407-323e-f274-e053-dbdaa90a6471Drug Facts
72133-051-022020-09-25C16284748780-1ab0e2407-323e-f274-e053-dbdaa90a6471Drug Facts
72133-051-082020-09-25C16284748780-1ab0e2407-323e-f274-e053-dbdaa90a6471Drug Facts
72133-051-122020-09-25C16284748780-1ab0e2407-323e-f274-e053-dbdaa90a6471Drug Facts
72133-051-022020-07-22C16284748780-1ab0e2407-323e-f274-e053-dbdaa90a6471Drug Facts
72133-051-082020-07-22C16284748780-1ab0e2407-323e-f274-e053-dbdaa90a6471Drug Facts
72133-051-122020-07-22C16284748780-1ab0e2407-323e-f274-e053-dbdaa90a6471Drug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72133-051PERSONAL CARE HAND SANITIZER WITH MOISTURIZERS VITAMIN E (ETHYL ALCOHOL) LIQUID [DELTA BRANDS & PRODUCTS LLC]1Legacy NDC20180407_6932a0dc-241f-42f0-e053-2991aa0adde5.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72133-05172133-051-08, 72133-051-12, 72133-051-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
6932a8b8-0a76-917a-e053-2991aa0a54f56932a0dc-241f-42f0-e053-2991aa0adde52018-04-06WarningsExact identifier
spl id: 6932a8b8-0a76-917a-e053-2991aa0a54f5
spl set id: 6932a0dc-241f-42f0-e053-2991aa0adde5

Reported adverse events (FAERS/openFDA)#

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