PROPOLIS HAND SANITIZER

Manufacturer: Iden Cosmetics, Inc.
Effective date: 2020-04-25
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:08:02

Label at a glance#

ProductPROPOLIS HAND SANITIZER

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

HAND SANITIZER TO HELP REDUCE BACTERIA THAT POTENTIALLY CAN CAUSE DISEASE. FOR USE WHEN SOAP AND WATER ARE NOT AVAILABLE.

Dosage and administration

PLACE ENOUGH PRODUCT ON HANDS TO COVER ALL SURFACES. RUB HANDS TOGETHER UNTIL DRY. SUPERVISE CHILDREN UNDER 6 YEARS OF AGE WHEN USING THIS PRODUCT TO AVOID SWALLOWING.

Storage and handling

STORE BETWEEN 15-30C (59-86F) AVOID FREEZING AND EXCESSIVE HEAT ABOVE 40C (104F)

Contacts and useful links#

PhoneLabel contact1-800-935-IDEN

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 70% V/V

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES

INDICATIONS & USAGE SECTION

HAND SANITIZER TO HELP REDUCE BACTERIA THAT POTENTIALLY CAN CAUSE DISEASE. FOR USE WHEN SOAP AND WATER ARE NOT AVAILABLE.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY. FLAMMABLE, KEEP AWAY FROM HEAT OR FLAME.

DO NOT USE

IN CHILDREN LESS THAN 2 MONTHS OF AGE
ON OPEN SKIN WOUNDS

WHEN USING THIS PRODUCT KEEP OUT OF EYES, EARS, AND MOUTH. IN CASE OF CONTACT WITH EYES, RINSE EYES THOROUGHLY WITH WATER.

STOP USE AND ASK A DOCTOR IF IRRITATION OR OR RASH OCCURS. THESE MAY BE SIGNS OF A SERIOUS CONDITION.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

PLACE ENOUGH PRODUCT ON HANDS TO COVER ALL SURFACES. RUB HANDS TOGETHER UNTIL DRY.
SUPERVISE CHILDREN UNDER 6 YEARS OF AGE WHEN USING THIS PRODUCT TO AVOID SWALLOWING.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

STORE BETWEEN 15-30C (59-86F)
AVOID FREEZING AND EXCESSIVE HEAT ABOVE 40C (104F)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER (AQUA), METHYL GLUCETH-20, CARBOMER, AMINOMETHYL PROPANOL, PROPOLIS EXTRACT, ALOE BARBADENSIS LEAF JUICE, CAMELLIA SINENSIS LEAF EXTRACT, GLYCERIN, TOCOPHERYL ACETATE

QUESTIONS?

OTC - QUESTIONS SECTION

1-800-935-IDEN * 1-800-935-4336

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Hand Sanitizer_4oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	3
581662	ethanol 0.7 ML/ML Topical Gel	SCD	3
581662	ethanol 70 % Topical Gel	SY	3
581662	ethyl alcohol 70 % Topical Gel	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74048-101-11	2022-01-28	C162847	48780-1	d6a99b39-6f73-a426-e053-dadaa90af4c2	IDEN BEE PROPOLIS - PROPOLIS HAND SANITIZER
74048-101-12	2022-01-28	C162847	48780-1	d6a99b39-6f73-a426-e053-dadaa90af4c2	IDEN BEE PROPOLIS - PROPOLIS HAND SANITIZER
74048-101-14	2022-01-28	C162847	48780-1	d6a99b39-6f73-a426-e053-dadaa90af4c2	IDEN BEE PROPOLIS - PROPOLIS HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
74048-101-11	PROPOLIS HAND SANITIZER	300 mL in 1 BOTTLE	GEL	300	3
74048-101-12	PROPOLIS HAND SANITIZER	1000 mL in 1 PACKAGE	GEL	1000	3
74048-101-14	PROPOLIS HAND SANITIZER	118 mL in 1 BOTTLE	GEL	118	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74048-101	PROPOLIS HAND SANITIZER (ETHYL ALCOHOL) GEL [IDEN COSMETICS, INC.]	3	Legacy NDC, 3 package rows	20200426_b97d2c7e-13cc-4bab-b061-4f85da20c9ad.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

PROPOLIS HAND SANITIZER
ETHYL ALCOHOL
ALCOHOL
WATER
METHYL GLUCETH-20
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
AMINOMETHYLPROPANOL
PROPOLIS WAX
ALOE VERA LEAF
GREEN TEA LEAF
GLYCERIN
.ALPHA.-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74048-101	74048-101-14, 74048-101-11, 74048-101-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
METHYL GLUCETH-20	J3QD0LD11P	IACT
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)	71DD5V995L	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
PROPOLIS WAX	6Y8XYV2NOF	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GREEN TEA LEAF	W2ZU1RY8B0	IACT
GLYCERIN	PDC6A3C0OX	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	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
8c22d36d-9994-4ba1-881c-c9b5bfd20c92			b97d2c7e-13cc-4bab-b061-4f85da20c9ad	2020-04-25	Warnings	Exact identifier spl id: 8c22d36d-9994-4ba1-881c-c9b5bfd20c92 spl set id: b97d2c7e-13cc-4bab-b061-4f85da20c9ad

Reported adverse events (FAERS/openFDA)#

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