Flod Hand Sanitizer Gel, Aloha-Green Apple Scent

Manufacturer
Aluma Packaging Corporation, S.A. de C.V.
Effective date
2022-03-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:48:43

Label at a glance#

ProductFlod Hand Sanitizer Gel, Aloha-Green Apple Scent
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Empty the contents of the packet into the palm of the hand, rub both hands until the product covers the entire surface of the hands, let it absorb. No need to rinse, wash or dry hands.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial Use

Use:

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin.

Warnings:

WARNINGS SECTION

Flammable, keep away from fire or flame. Exclusively for external use.  Do not ingest, in case of accidental ingestion consult your doctor immediately. Keep away from the eyes, in case of accidental contact with eyes, rinse with water and consult your doctor. In case of irritation or redness, discontinue use, if discomfort persists consult your doctor.

Keep out of reach of children,

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

supervision is required for children under 6 years of age.

Directions:

DOSAGE & ADMINISTRATION SECTION

Empty the contents of the packet into the palm of the hand, rub both hands until the product covers the entire surface of the hands, let it
absorb. No need to rinse, wash or dry hands.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water, carbomer, triethanolamine, glycerin, Castor Oil, tocopheryl acetate, Aloe vera extract. Fragrance.

Other information:

SPL UNCLASSIFIED SECTION

Store below 110ºF (43ºC)

Questions or comments:

OTC - QUESTIONS SECTION

a.comercial@alumpack.com

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabel2Label2Label3Label3Label4Label4Label5Label5

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81998-001-012023-07-28C16284748780-10191ceaa-6d08-198a-e063-dbdaa90aec3eFlod Hand Sanitizer Gel, Aloha-Green Apple Scent

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81998-001-01Flod Hand Sanitizer Gel, Aloha-Green Apple Scent100 in 1 PACKETGEL1002
81998-001-01Flod Hand Sanitizer Gel, Aloha-Green Apple Scent12 in 1 BOXGEL122

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81998-001FLOD HAND SANITIZER GEL, ALOHA-GREEN APPLE SCENT (ALCOHOL) GEL [ALUMA PACKAGING CORPORATION, S.A. DE C.V.]2Legacy NDC, 2 package rows20220311_c469df98-ec0e-2c76-e053-2a95a90af006.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81998-00181998-001-01
77739-001

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
d9cdf987-c8a5-c429-e053-2995a90ae074c469df98-ec0e-2c76-e053-2a95a90af0062022-03-09WarningsExact identifier
spl id: d9cdf987-c8a5-c429-e053-2995a90ae074
spl set id: c469df98-ec0e-2c76-e053-2a95a90af006

Reported adverse events (FAERS/openFDA)#

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