AlcoMax

Manufacturer
CONIC CO., LTD. | CONIC CO., LTD
Effective date
2020-11-25
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:34:14

Label at a glance#

ProductAlcoMax
Active ingredientALCOHOL
Label structure12 sections

Storage and handling

Store between 33.8~86'F Avoid freezing and excessive heat

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

ALCHOL 70%

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis leaf, chamaecyparis Obtusa leaf, Glycerin, Carbomer, Arqinine, DISODIUM EDTA

Direction

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.

Do not use

OTC - DO NOT USE SECTION

In children less than 2 months of age .

On open skin wounds

When using this product

OTC - WHEN USING SECTION

Keep out of eyes, ears, and mouth in case of contact with eyes, rinse eyes thoroughly whit water.

Warnings

WARNINGS SECTION

for external sue only. Flammable. keep away from heat or flame

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.

Stop use and ask a doctor.

OTC - STOP USE SECTION

if irritationor rash occurs. These may be signs of a serious contion.

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not avaliable.

Other information

STORAGE AND HANDLING SECTION

Store between 33.8~86'F

Avoid freezing and excessive heat

Pakage Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

​3.7L 75700-301-04

100ml 75700-301-03

500ml 75700-301-02 (new)

500ml 75700-301-01

1gal label(3.7L)1gal label(3.7L)

100ml label100ml label

new label image 500mlnew label image 500ml

500ml NDC:75700-301-01 Label500ml NDC:75700-301-01 Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN4
581662ethanol 0.7 ML/ML Topical GelSCD4
581662ethanol 70 % Topical GelSY4
581662ethyl alcohol 70 % Topical GelSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75700-301-01AlcoMax500 mL in 1 BOTTLE, PUMPGEL5004
75700-301-02AlcoMax500 mL in 1 BOTTLE, PUMPGEL5004
75700-301-03AlcoMax100 mL in 1 TUBEGEL1004
75700-301-04AlcoMax3700 mL in 1 BOTTLE, PUMPGEL37004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75700-301ALCOMAX (ALCOHOL) GEL [CONIC CO., LTD.]4Legacy NDC, 4 package rows20201126_a39ccce4-eb8c-d850-e053-2995a90a25d4.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
75700-30175700-301-01, 75700-301-02, 75700-301-03, 75700-301-04

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 · 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
b4e95a9f-45bc-587c-e053-2a95a90a1628a39ccce4-eb8c-d850-e053-2995a90a25d42020-11-25WarningsExact identifier
spl id: b4e95a9f-45bc-587c-e053-2a95a90a1628
spl set id: a39ccce4-eb8c-d850-e053-2995a90a25d4

Reported adverse events (FAERS/openFDA)#

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