Hand Sanitizing Wipes

Manufacturer: PHOENIX HEALTHCARE SOLUTIONS, LLC | Phoenix Innovative Healthcare Manufacturers Private Limited
Effective date: 2025-10-23
Label type: HUMAN OTC DRUG LABEL
Version: 8
Source: full-release
Hydrated at: 2026-06-01 01:40:35

Label at a glance#

ProductHand Sanitizing Wipes

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin

Dosage and administration

Unfold towelette; Wipe hands; Discard after use

Storage and handling

■ Store at room temperature: 15℃~30℃(59℉~86℉) ■ May discolor certain fabrics or surfaces

Contacts and useful links#

PhoneLabel contact+1-954-607-6080

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

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.

When using this product

OTC - WHEN USING SECTION

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

Discontinue use and ask a doctor if

OTC - ASK DOCTOR SECTION

■ Irritation or rash appears and lasts.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Unfold towelette; Wipe hands; Discard after use

Inactive ingredient

INACTIVE INGREDIENT SECTION

Purified Water

Other information

STORAGE AND HANDLING SECTION

■ Store at room temperature: 15℃~30℃(59℉~86℉)
■ May discolor certain fabrics or surfaces

Questions

OTC - QUESTIONS SECTION

+1-954-607-6080

Other Information

SPL UNCLASSIFIED SECTION

KILLS 99.99% OF GERMS*

Single Use Only

Do Not Flush

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 60913-415-11

Alcohol Formula, Fragrance Free, Paraben Free

Phoenix Healthcare Solutions, LLC

"An Innovative Medical Manufacturer"

HAND SANITIZING WIPES

KILLS 99.99% OF GERMS*

5.1 in. X 5.9 in. (13 cm X 15 cm)

110 INDIVIDUALLY WRAPPED WIPES

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041780	ethanol 62 % Medicated Pad	PSN	8
1041780	ethanol 0.62 ML/ML Medicated Pad	SCD	8
1041780	ethanol 62 % Hand Sanitizer Wipes	SY	8
1041780	ethanol 62 % Medicated Pad	SY	8
1041780	ethanol 62 % Topical Cloth	SY	8
1041780	ethanol 62 % Topical Swab	SY	8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60913-415-11	Hand Sanitizing Wipes	1 mL in 1 PACKET	CLOTH	1		8
60913-415-11	Hand Sanitizing Wipes	110 in 1 BOX	CLOTH	110		8

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
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60913-415	60913-415-11

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
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
7	2024-10-17	full-release	2026-06-01 00:27:15

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
Hand Sanitizing Wipes	ETHYL ALCOHOL	PHOENIX HEALTHCARE SOLUTIONS, LLC	ca9f8e68-cc15-42b4-81fd-e114e6a6d7df	2025-10-23	Warnings	Exact identifier ndc (package): 60913-415-11 ndc (product): 60913-415 ndc11 (package): 60913041511 spl id: 41d17fa3-30eb-4bdd-e063-6394a90a2654 spl set id: ca9f8e68-cc15-42b4-81fd-e114e6a6d7df

Reported adverse events (FAERS/openFDA)#

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