I BEBE

Manufacturer: I MEDISON CO., LTD.
Effective date: 2020-04-13
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:06:10

Label at a glance#

ProductI BEBE

Active ingredientALCOHOL

Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

alcohol

INACTIVE INGREDIENT SECTION

Purified Water, Carbomer, sodium hyaluronate, glycerin, aloe X

OTC - PURPOSE SECTION

Antimicrobial

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

WARNINGS SECTION

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	2
581662	ethanol 0.7 ML/ML Topical Gel	SCD	2
581662	ethanol 70 % Topical Gel	SY	2
581662	ethyl alcohol 70 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74650-0002-1	2022-01-28	C162847	48780-1	d6a99b39-547b-a426-e053-dadaa90af4c2	Drug Facts
74650-0002-2	2022-01-28	C162847	48780-1	d6a99b39-547b-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74650-0002-1	I BEBE	160 mL in 1 BOTTLE	GEL	160		2
74650-0002-2	I BEBE	360 mL in 1 BOTTLE	GEL	360		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74650-0002	I BEBE (ALCOHOL) GEL [I MEDISON CO., LTD.]	2	Legacy NDC, 2 package rows	20200414_a312d258-1f9d-4f99-e053-2a95a90af304.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

I BEBE
alcohol
ALOE VERA LEAF
HYALURONATE SODIUM
CARBOMER 940
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74650-0002	74650-0002-1, 74650-0002-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
HYALURONATE SODIUM	YSE9PPT4TH	IACT
CARBOMER 940	4Q93RCW27E	IACT
WATER	059QF0KO0R	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
a3358082-9325-4832-e053-2995a90a015b			a312d258-1f9d-4f99-e053-2a95a90af304	2020-04-13	Warnings	Exact identifier spl id: a3358082-9325-4832-e053-2995a90a015b spl set id: a312d258-1f9d-4f99-e053-2a95a90af304

Reported adverse events (FAERS/openFDA)#

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