Sanimax Hand Sanitizer

Manufacturer: AK-PAK-Ricci
Effective date: 2020-06-29
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:20:22

Label at a glance#

ProductSanimax Hand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire and flame.

Do not use

OTC - DO NOT USE SECTION

■ on 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 eye contact, immediately flush eyes thoriughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash occurs. These may be signs of a serious condition

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidential ingestion, contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

SPL UNCLASSIFIED SECTION

■ Store between 15º- 30º (59-86ºF). ■ Avoid freezing and excessive heat above 40º (104ºF) ■ May discolor fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

aloe extract, glycerin, isopropyl alcohol, isopropyl myristate, polyacrylic acid, propylene glycol, tocopheryl acetate, water.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74585-001-01	2022-01-28	C162847	48780-1	d6a99b39-425e-a426-e053-dadaa90af4c2	Sanimax Hand Sanitizer
74585-001-02	2022-01-28	C162847	48780-1	d6a99b39-425e-a426-e053-dadaa90af4c2	Sanimax Hand Sanitizer
74585-001-03	2022-01-28	C162847	48780-1	d6a99b39-425e-a426-e053-dadaa90af4c2	Sanimax Hand Sanitizer
74585-001-08	2022-01-28	C162847	48780-1	d6a99b39-425e-a426-e053-dadaa90af4c2	Sanimax Hand Sanitizer
74585-001-28	2022-01-28	C162847	48780-1	d6a99b39-425e-a426-e053-dadaa90af4c2	Sanimax Hand Sanitizer
74585-001-33	2022-01-28	C162847	48780-1	d6a99b39-425e-a426-e053-dadaa90af4c2	Sanimax Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
74585-001-01	Sanimax Hand Sanitizer	30 mL in 1 BOTTLE, PLASTIC	LIQUID	30	2
74585-001-02	Sanimax Hand Sanitizer	60 mL in 1 BOTTLE, PLASTIC	LIQUID	60	2
74585-001-03	Sanimax Hand Sanitizer	3 in 1 PACKAGE	LIQUID	3	2
74585-001-08	Sanimax Hand Sanitizer	236 mL in 1 BOTTLE, PLASTIC	LIQUID	236	2
74585-001-28	Sanimax Hand Sanitizer	3780 mL in 1 BOTTLE, PLASTIC	LIQUID	3780	2
74585-001-33	Sanimax Hand Sanitizer	1000 mL in 1 BOTTLE, PLASTIC	LIQUID	1000	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74585-001	SANIMAX HAND SANITIZER (ALCOHOL) LIQUID [AK-PAK-RICCI]	2	Legacy NDC, 6 package rows	20200708_a341a3c8-9ecc-52e9-e053-2995a90a300f.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Sanimax Hand Sanitizer
Alcohol
ALOE
GLYCERIN
WATER
ISOPROPYL MYRISTATE
ISOPROPYL ALCOHOL
.ALPHA.-TOCOPHEROL ACETATE
PROPYLENE GLYCOL
POLYACRYLIC ACID (250000 MW)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74585-001	74585-001-02, 74585-001-08, 74585-001-01, 74585-001-33, 74585-001-28, 74585-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE	V5VD430YW9	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
ALCOHOL	3K9958V90M	ACTIB
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
POLYACRYLIC ACID (250000 MW)	9G2MAD7J6W	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a939b3a7-1b72-c815-e053-2a95a90a615b			a341a3c8-9ecc-52e9-e053-2995a90a300f	2020-06-29	Warnings	Exact identifier spl id: a939b3a7-1b72-c815-e053-2a95a90a615b spl set id: a341a3c8-9ecc-52e9-e053-2995a90a300f

Reported adverse events (FAERS/openFDA)#

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