Skin Cottage 70 Percent Ethyl Alcohol Antiseptic Hand Sanitizer

Manufacturer: KEN-RICH CORPORATION SDN. BHD.
Effective date: 2024-07-11
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 00:15:20

Label at a glance#

ProductSkin Cottage 70 Percent Ethyl Alcohol Antiseptic Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Contacts and useful links#

PhoneLabel contact775-225-9908

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

in the eyes.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

Irritation and redness develop.
Condition persists for more than 72 hours.

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

Wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, propylene glycol, acrylates/C10-30 alkyl acrylate crosspolymer, triethanolamine.

Questions or Comments?

OTC - QUESTIONS SECTION

775-225-9908

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	4
581662	ethanol 0.7 ML/ML Topical Gel	SCD	4
581662	ethanol 70 % Topical Gel	SY	4
581662	ethyl alcohol 70 % Topical Gel	SY	4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79468-001-01	2026-01-29	C162847	48780-1	1030e365-10d6-111a-e063-dadaa90a10e2	Skin Cottage 70% Ethyl Alcohol Antiseptic Hand Sanitizer
79468-001-01	2024-01-30	C162847	48780-1	1030e365-10d6-111a-e063-dadaa90a10e2	Skin Cottage 70% Ethyl Alcohol Antiseptic Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79468-001-01	Skin Cottage 70 Percent Ethyl Alcohol Antiseptic Hand Sanitizer	500 mL in 1 BOTTLE	GEL	500		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79468-001	SKIN COTTAGE 70 PERCENT ETHYL ALCOHOL ANTISEPTIC HAND SANITIZER (ALCOHOL) GEL [KEN-RICH CORPORATION SDN. BHD.]	4	Legacy NDC, 1 package rows	20240716_b09d4e16-1993-cdeb-e053-2a95a90ae2db.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Skin Cottage 70 Percent Ethyl Alcohol Antiseptic Hand Sanitizer
ALCOHOL
WATER
GLYCERIN
PROPYLENE GLYCOL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79468-001	79468-001-01

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
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
TROLAMINE	9O3K93S3TK	IACT
ALCOHOL	3K9958V90M	ACTIB

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
1cf9d603-26e5-1223-e063-6394a90a9e65			b09d4e16-1993-cdeb-e053-2a95a90ae2db	2024-07-11	Warnings	Exact identifier spl id: 1cf9d603-26e5-1223-e063-6394a90a9e65 spl set id: b09d4e16-1993-cdeb-e053-2a95a90ae2db

Reported adverse events (FAERS/openFDA)#

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