Pharmacys Prescription Hand Sanitizer

Manufacturer: American Consumer Products Corp
Effective date: 2020-08-14
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:24:41

Label at a glance#

ProductPharmacys Prescription Hand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Indications and uses

Uses - Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

Directions - apply as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients - Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Uses - Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings

WARNINGS SECTION

Warnings - For external use only. Do not ingest or swallow.

Flammable. Keep away from fire or flame.

Do not appy around eyes. Do not use in ears & mouth.

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Do not use on children less than 2 months of age. Supervise use in children under 6 years of age to prevent accidental swallowing. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions - apply as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Other information

SPL UNCLASSIFIED SECTION

Other information - store at 20º C (68º to 77º F). May discolor fabrics.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Purified Water (Aqua), Carbomer, Aminomethyl Propanol, Tocopheryl Acetate (Vitamin E), Aloe Barbadensis (Aloe Vera) Leaf Juice

Pharmacys Prescription Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0087508213989	GTIN-13: 0087508213989 EAN-13: 0087508213989 GTIN-12: 087508213989 UPC-A: 087508213989 GTIN storage (14 digits): 00087508213989	72197-034-99_Hand_Sanitizer.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72197-034-99	2022-01-28	C162847	48780-1	d6a99b39-e045-a426-e053-dadaa90af4c2	Pharmacys Prescription Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72197-034-99	Pharmacys Prescription Hand Sanitizer	3785.41 mL in 1 BOTTLE	GEL	3785.41		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72197-034	PHARMACYS PRESCRIPTION HAND SANITIZER (ALCOHOL) GEL [AMERICAN CONSUMER PRODUCTS CORP]	1	Legacy NDC, 1 package rows	20200814_acc52277-009b-e8cc-e053-2a95a90a2e7b.zip

Products#

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

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

Pharmacys Prescription Hand Sanitizer
Alcohol
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
ALOE VERA LEAF
WATER
AMINOMETHYLPROPANOL
.ALPHA.-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72197-034	72197-034-99

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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
ALCOHOL	3K9958V90M	ACTIB
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT

Source Document#

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
acc50bec-d6f5-61e2-e053-2995a90a0db4			acc52277-009b-e8cc-e053-2a95a90a2e7b	2020-08-14	Warnings	Exact identifier spl id: acc50bec-d6f5-61e2-e053-2995a90a0db4 spl set id: acc52277-009b-e8cc-e053-2a95a90a2e7b

Reported adverse events (FAERS/openFDA)#

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