NDC- 63148-114-08, DDMart

Manufacturer
Apollo Health and Beauty Care
Effective date
2026-05-03
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:56:08

Label at a glance#

ProductDD Mart Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

For Personal hand hygiene to help the spread of bacteria and can be used in place of hand washing if soap and water are not available.

Dosage and administration

For occasional and personal use Rub thoroughly into hands for at least 30 seconds. Allow to dry Children under 6 years should be supervised when using this product

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For Personal hand hygiene to help the spread of bacteria and can be used in place of hand washing if soap and water are not available.

Warnings

WARNINGS SECTION

  • For External use only
  • Flammable
  • Keep away from source of heat or fire.

Do Not use

OTC - DO NOT USE SECTION

  • on infants less than 2 months of age
  • on open skin wounds
  • on broken or damaged skin

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
  • Do not Inhale.

Stop use and ask a doctor

OTC - STOP USE SECTION

If Irritation or redness develops and lasts.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Centre immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • For occasional and personal use
  • Rub thoroughly into hands for at least 30 seconds. Allow to dry
  • Children under 6 years should be supervised when using this product

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Eau), PEG-6, AMP-Acrylates/Vinyl Isodecanoate Crosspolymer, Fragrance (Parfum), Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Isopropyl Alcohol, Isopropyl Myristate.

Label copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DD MartDD Mart

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN7
582753ethanol 0.7 ML/ML Topical SolutionSCD7
582753ethanol 70 % Topical SolutionSY7
582753ethyl alcohol 70 % Topical SolutionSY7

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130093351037887GTIN-13: 0093351037887
EAN-13: 0093351037887
GTIN-12: 093351037887
UPC-A: 093351037887
GTIN storage (14 digits): 00093351037887
06-26491-92.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63148-114-08DD Mart Hand Sanitizer236 mL in 1 BOTTLE, PLASTICLIQUID2367

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63148-11463148-114-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
DD Mart Hand SanitizerALCOHOLApollo Health and Beauty Care0b1806c2-2469-0c81-e063-6394a90a3b2a2026-05-03WarningsExact identifier
ndc (package): 63148-114-08
ndc (product): 63148-114
ndc11 (package): 63148011408
spl id: 50ec5872-bf51-3be1-e063-6394a90a1311
spl set id: 0b1806c2-2469-0c81-e063-6394a90a3b2a

Reported adverse events (FAERS/openFDA)#

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