FOAMING HAND

Manufacturer: Draco Hygienic Products Inc.
Effective date: 2024-10-08
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:23:11

Label at a glance#

ProductFOAMING HAND ALCOHOL FOAM

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

Place enough product on your palm to thoroughly cover your hands. Rub hands together briskly until dry.

Storage and handling

Store below 110° (43°C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70% W/W

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.

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use this product 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
lf swallowed,get medical help or contact Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Place enough product on your palm to thoroughly cover your hands.
Rub hands together briskly until dry.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store below 110° (43°C)
May discolor certain fabrics or surfaces

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water (Aqua), Isopropyl Alcohol, Propylene Glycol, Glycerin, Polyaminopropyl Biguanide, PEG-10 Dimethicone, Isopropyl Myristate, Butyrospermum Parkii (Shea Butter)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

lbl

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616805	ethanol 70 % Topical Foam	PSN	2
616805	ethanol 0.7 ML/ML Topical Foam	SCD	2
616805	ethanol 70 % Topical Foam	SY	2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83019-102-11	FOAMING HANDALCOHOL FOAM	1000 mL in 1 CONTAINER	SOAP	1000		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83019-102	FOAMING HAND ALCOHOL FOAM (ALCOHOL) SOAP [DRACO HYGIENIC PRODUCTS INC.]	2	Current NDC, 1 package rows	20241010_14860a19-e1e8-71fc-e063-6394a90a9df8.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

FOAMING HAND ALCOHOL FOAM
ALCOHOL
POLYAMINOPROPYL BIGUANIDE
ISOPROPYL MYRISTATE
SHEA BUTTER
WATER
ISOPROPYL ALCOHOL
PROPYLENE GLYCOL
GLYCERIN
PEG-10 DIMETHICONE (200 CST)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83019-102	83019-102-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POLYAMINOPROPYL BIGUANIDE	DT9D8Z79ET	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
SHEA BUTTER	K49155WL9Y	IACT
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
GLYCERIN	PDC6A3C0OX	IACT
PEG-10 DIMETHICONE (200 CST)	287GF3Y3WC	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
FOAMING HAND ALCOHOL FOAM	ALCOHOL	Draco Hygienic Products Inc.	14860a19-e1e8-71fc-e063-6394a90a9df8	2024-10-08	Warnings	Exact identifier ndc (package): 83019-102-11 ndc (product): 83019-102 ndc11 (package): 83019010211 spl id: 23f92979-e918-8620-e063-6294a90a9790 spl set id: 14860a19-e1e8-71fc-e063-6394a90a9df8

Reported adverse events (FAERS/openFDA)#

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