SEPHORA BY OPI MOISTURIZING HAND SANITIZER SPRAY

Manufacturer
OPI Products Inc. | OPI Products Inc
Effective date
2010-07-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:52:44

Label at a glance#

ProductSEPHORA BY OPI MOISTURIZING HAND SANITIZER
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts
Active Ingredients             Purpose
Alcohol 65%....................Antimicrobial

OTC - PURPOSE SECTION

Uses
• hand sanitizer to help
reduce bacteria on hands
and skin
• recommended for repeated
use

WARNINGS SECTION

Warnings
For External use only.
Flammable, keep away
from fire or flame.

OTC - DO NOT USE SECTION

Do not use
• in the eyes. In case of
contact, rinse eyes
thoroughly with water
• on deep or puncture
wounds

OTC - STOP USE SECTION

Stop use and consult a
physician if irritation and
sensitization develop and
persist for more than 72
hours.

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.

DOSAGE & ADMINISTRATION SECTION

Directions
• spray hands thoroughly
with product
• allow to dry without wiping
• supervise children in the
use of this product

INACTIVE INGREDIENT SECTION

Inactive Ingredients
water/aqua/eau, PEG-8
dimethicone, denatonium
benzoate, t-butyl alcohol.
parfum/ fragrance, benzyl,
salicylate, coumarin,
limoene, butylphenyl,
methylpropional, linalool.

SPL UNCLASSIFIED SECTION

Questions or Comments?
Call toll free Mon-Fri
1-800-341-9999

Made Exclusively for
Sephora by OPI
© 2010 • Ver. 10-0230
Item No. SE 558
Distributed by Sephora USA,
San Francisco, CA 94105
www.sephora.com
Made in USA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

moisturizing hand sanitizer spray
Kills 99% of germs on contact without using water

SEPHORA by OPI

moisturizing hand sanitizer spray

8ml - 0.27fl oz e

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

handsanitizerlabelhandsanitizerlabel

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1
BENZYL SALICYLATEINACTIVE INGREDIENTWAO5MNK9TU1
BUTYLPHENYL METHYLPROPIONALINACTIVE INGREDIENTT7540GJV691
COUMARININACTIVE INGREDIENTA4VZ22K1WT1
DENATONIUM BENZOATEINACTIVE INGREDIENT4YK5Z54AT21
LINALOOL, DL-INACTIVE INGREDIENTD81QY6I88E1
TERT-BUTYL ALCOHOLINACTIVE INGREDIENTMD83SFE9591
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61852-63761852-637-08

Ingredients#

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

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

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
TERT-BUTYL ALCOHOLTERT-BUTYL ALCOHOLMD83SFE959GEL / TOPICAL0.12 %w/wExact identifier — unii candidate
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2GEL / TOPICALNAExact identifier — unii candidate
3 equally ranked IID candidates
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2SWAB / TOPICALNAExact identifier — unii candidate
3 equally ranked IID candidates
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2SOLUTION / TOPICALNAExact identifier — unii candidate
3 equally ranked IID candidates

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f18a098c-c3b9-4555-e053-2a95a90a73283477e84a-0597-4e99-afa0-d9cd51544c122023-01-05WarningsExact identifier
spl set id: 3477e84a-0597-4e99-afa0-d9cd51544c12

Reported adverse events (FAERS/openFDA)#

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