Natura Gel

Manufacturer
Ad Medios & Mkt, S.A. de C.V.
Effective date
2020-06-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:18

Label at a glance#

ProductNatura Gel
Active ingredientALCOHOL
Label structure19 sections

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

OTC - DO NOT USE SECTION

in children less than 2 months of age
on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENT SECTION

polyacrylic acid (Carbomer), triethanolamine (Trolamine), water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 ML60 ML60 ml NDC 79058-001-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

250 ML250 ML250 ML NDC: 79058-001-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500 ml NDC: 79058-001-03 500 ml500 ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1000 ml1000 ml1000 ML NDC:79058-001-04

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3785 ml3785 ml3785 ML NDC:79085-001-05

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5 L5 L5000 ML NDC:79058-001-06

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20 L20 L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

200 L200 L200,000 ML NDC: 79058-001-08

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79058-001-01Natura Gel60 mL in 1 BOTTLEGEL601
79058-001-02Natura Gel250 mL in 1 BOTTLEGEL2501
79058-001-03Natura Gel500 mL in 1 BOTTLEGEL5001
79058-001-04Natura Gel1000 mL in 1 BOTTLEGEL10001
79058-001-05Natura Gel3785 mL in 1 BOTTLEGEL37851
79058-001-06Natura Gel5000 mL in 1 BOTTLEGEL50001
79058-001-07Natura Gel20000 mL in 1 BOTTLEGEL200001
79058-001-08Natura Gel200000 mL in 1 BOTTLEGEL2000001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79058-001NATURA GEL (ALCOHOL) GEL [AD MEDIOS & MKT, S.A. DE C.V.]1Legacy NDC, 8 package rows20200619_a84ff942-d6d0-5d8d-e053-2a95a90aa8d2.zip

Products#

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

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

NDC Codes#

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

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
a84ff942-d6d1-5d8d-e053-2a95a90aa8d2a84ff942-d6d0-5d8d-e053-2a95a90aa8d22020-06-17WarningsExact identifier
spl id: a84ff942-d6d1-5d8d-e053-2a95a90aa8d2
spl set id: a84ff942-d6d0-5d8d-e053-2a95a90aa8d2

Reported adverse events (FAERS/openFDA)#

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