RN Wellness Sanitizer

Manufacturer: RN Wellness
Effective date: 2020-07-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:20:57

Label at a glance#

ProductRN Wellness Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

-For hand washing to decrease bacteria on skin. -Recommended for repeated use

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping -Do not use other than directed

Storage and handling

Store at room temperature 20-25 °C (66-77 °F)

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70%

Purpose:

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

-For hand washing to decrease bacteria on skin.

-Recommended for repeated use

WARNINGS:

WARNINGS SECTION

-Flammable, keep away from fire or flame.

OTC - WHEN USING SECTION

-For external use only.

OTC - DO NOT USE SECTION

-Do not use in eyes. If contact occurs, flush thoroughly with water

OTC - ASK DOCTOR SECTION

-Stop use and ask a doctor if redness and irritation develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

-Directions:

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

-Do not use other than directed

STORAGE AND HANDLING SECTION

Store at room temperature 20-25 °C (66-77 °F)

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aqua, Glycerin, Tocopherol.

59.15 mL NDC: 79556-123-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RN Wellness Hand Sanitizer Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79556-123-02	2021-07-23	C162847	48780-1	c7ccaba7-11a9-fd44-e053-dadaa90aa01b	a97d0099-c8e0-37c7-e053-2995a90a8576

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79556-123-02	RN Wellness Sanitizer	59.15 mL in 1 BOTTLE, SPRAY	LIQUID	59.15		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79556-123	RN WELLNESS SANITIZER (ETHYL ALCOHOL) LIQUID [RN WELLNESS]	1	Legacy NDC, 1 package rows	20200711_a97d0099-c8e0-37c7-e053-2995a90a8576.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

RN Wellness Sanitizer
Ethyl Alcohol
THYME OIL
ALCOHOL
WATER
ORANGE OIL
GLYCERIN
.ALPHA.-TOCOPHEROL, DL-

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79556-123	79556-123-02
74306-133

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
THYME OIL	2UK410MY6B	IACT
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
ORANGE OIL	AKN3KSD11B	IACT
GLYCERIN	PDC6A3C0OX	IACT
.ALPHA.-TOCOPHEROL, DL-	7QWA1RIO01	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
a97d0099-c8e1-37c7-e053-2995a90a8576			a97d0099-c8e0-37c7-e053-2995a90a8576	2020-07-10	Warnings	Exact identifier spl id: a97d0099-c8e1-37c7-e053-2995a90a8576 spl set id: a97d0099-c8e0-37c7-e053-2995a90a8576

Reported adverse events (FAERS/openFDA)#

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