MDmaxx Hand Sanitizing Wipes

Manufacturer: Phoenix Healthcare Solutions LLC | Phoenix Innovative Healthcare Manufacturers Private Limited
Effective date: 2026-11-03
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: daily-update
Hydrated at: 2026-11-06 02:02:19

Label at a glance#

ProductHand Sanitizing Wipes

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

Unfold towelette; wipe hands; discard after use.

Storage and handling

Store between 15C -30C (59F-86F) May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

OTC - WHEN USING SECTION

When using this product

Do not use in or near the eyes. In case of contact rinse eyes thouroughly with water.

Discontinue use and ask a doctor if irritation or rash appears and lasts.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Unfold towelette; wipe hands; discard after use.

Other information

STORAGE AND HANDLING SECTION

Store between 15C -30C (59F-86F)
May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Box

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Hand Sanitizing Wipes
ETHYL ALCOHOL
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60913-416	60913-416-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
6	2025-10-23	full-release	2026-06-01 01:40:34
5	2024-10-17	full-release	2026-06-01 00:27:13

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
41d1600b-d58f-a36f-e063-6294a90afa23			c68d2d73-be78-8e1c-e053-2995a90a3a37	2025-10-23	Warnings	Exact identifier spl set id: c68d2d73-be78-8e1c-e053-2995a90a3a37

Reported adverse events (FAERS/openFDA)#

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