very vanilla

Manufacturer: Huijing (Shanghai) Bio-tech Co., Ltd
Effective date: 2017-06-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:51:44

Label at a glance#

Productvery vanilla

Active ingredientALCOHOL

Label structure12 sections

Storage and handling

Other Information Store below 110° F (43° C)

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Inactive Ingredients

carbomer 940, glycerin,

propylene glycol, red 33,

tocopheryl acetate,

triethanolamine, water

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl Alcohol 65 % v/v

OTC - PURPOSE SECTION

Purpose Antimicrobial

WARNINGS SECTION

Warnings

For external use only.

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.

INDICATIONS & USAGE SECTION

Uses

hand sanitizer to reduce bacteria on skin

DOSAGE & ADMINISTRATION SECTION

Directions Put a dime sized drop onto hands

and rub together briskly until dry.

OTC - DO NOT USE SECTION

Do not use in or near the eyes.

In case of contact, rinse eyes

thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor

if irritation, excessive redness or

rash develops.

OTHER SAFETY INFORMATION

Flammable. Keep away from

fire or flame.

STORAGE AND HANDLING SECTION

Other Information

Store below 110° F (43° C)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
902574	ethanol 65 % Topical Gel	PSN	1
902574	ethanol 0.65 ML/ML Topical Gel	SCD	1
902574	ethyl alcohol 65 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71537-004-01	2020-01-31	C162847	48780-1	9d75b9cf-dc22-f424-e053-dadaa90a57ce	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71537-004-01	very vanilla	29 mL in 1 BOTTLE, PLASTIC	GEL	29		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71537-004	VERY VANILLA (ETHYL ALCOHOL) GEL [HUIJING (SHANGHAI) BIO-TECH CO., LTD]	1	Legacy NDC, 1 package rows	20170627_cb4ad9f3-ee7e-4bae-b79f-811b0ec60467.zip

Products#

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

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

very vanilla
Ethyl Alcohol
ALCOHOL
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)
GLYCERIN
PROPYLENE GLYCOL
D&C RED NO. 33
.ALPHA.-TOCOPHEROL ACETATE
TROLAMINE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71537-004	71537-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)	4Q93RCW27E	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
D&C RED NO. 33	9DBA0SBB0L	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
TROLAMINE	9O3K93S3TK	IACT
WATER	059QF0KO0R	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
84f1caba-9642-4c81-aeb7-c2254163c766			cb4ad9f3-ee7e-4bae-b79f-811b0ec60467	2017-06-26	Warnings	Exact identifier spl id: 84f1caba-9642-4c81-aeb7-c2254163c766 spl set id: cb4ad9f3-ee7e-4bae-b79f-811b0ec60467

Reported adverse events (FAERS/openFDA)#

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