Nature Drops Hand Sanitizer

Manufacturer
Bioplasticos y Polimeros BIOFASE, S.A.P.I. de C.V.
Effective date
2020-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:29

Label at a glance#

ProductNature Drops Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand Sanitizer to help reduce germs. For use when soap and water not available.

Dosage and administration

Apply a small amount of product into hands and rub between both side of hands until dry. Supervise children under 6 years of age when using this product to avoid swalloing.

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol at 70%

Purpose:

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce germs. For use when soap and water not available.

Warnings:

WARNINGS SECTION

For external use only, Flammable. Keep away from open flame and sources of heat or flame.

Do not use:

OTC - DO NOT USE SECTION

In children less than 2 months of age. Open skinwounds.

When using this product:

OTC - WHEN USING SECTION

Keep out of eyes, ears, and mouth. In case of contact with eyes,rinse immediately with plenty of water and seek medical advice.

Stop use and ask doctor:

OTC - STOP USE SECTION

If an irritation or rash occurs.

Keep out of reach of children:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical advice or contact a poison control center immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply a small amount of product into hands and rub between both side of hands until dry. Supervise children under 6 years of age when using this product to avoid swalloing.

Other information:

SPL UNCLASSIFIED SECTION

Store below 110ºF (43ºC). Avoid freezing. May discolor certain fabrics or surface.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Glycerin, Hydroxyethyl Cellulose, fragance.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77452-001-012022-01-28C16284748780-1d6a99b39-d8ea-a426-e053-dadaa90af4c2Nature Drops Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77452-001-01Nature Drops Hand Sanitizer1000 mL in 1 BOTTLELIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77452-001NATURE DROPS HAND SANITIZER (ALCOHOL) LIQUID [BIOPLASTICOS Y POLIMEROS BIOFASE, S.A.P.I. DE C.V.]1Legacy NDC, 1 package rows20200509_b62404db-cf7d-4dc1-b299-25c60b5abef2.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77452-00177452-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML · Source PDF

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
a5248d35-f48b-3457-e053-2995a90a411eb62404db-cf7d-4dc1-b299-25c60b5abef22020-05-08WarningsExact identifier
spl id: a5248d35-f48b-3457-e053-2995a90a411e
spl set id: b62404db-cf7d-4dc1-b299-25c60b5abef2

Reported adverse events (FAERS/openFDA)#

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