FDA.reportPublic FDA data

The creme shop MOISTURIZING SANITIZER SRPAY Strawberry Scented

Manufacturer
MPRBRAIN CO.LTD
Effective date
2020-10-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:19

Label at a glance#

ProductThe creme shop MOISTURIZING SANITIZER SRPAY Strawberry Scented
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The creme shop Moisturizing Sanitizer SANITIZER SRPAY Strawberry ScentedThe creme shop Moisturizing Sanitizer SANITIZER SRPAY Strawberry Scented

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN1
1041849ethanol 0.7 ML/ML Topical SpraySCD1
1041849ethanol 70 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74741-1170-12023-01-30C16284748780-1f386c64a-1371-0266-e053-dadaa90a7c1aThe creme shop MOISTURIZING SANITIZER SRPAY Strawberry Scented 74741-1170-1 Bottle+Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74741-1170-1The creme shop MOISTURIZING SANITIZER SRPAY Strawberry Scented100 mL in 1 BOTTLE, SPRAYSPRAY1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74741-1170THE CREME SHOP MOISTURIZING SANITIZER SRPAY STRAWBERRY SCENTED (ETHYL ALCOHOL) SPRAY [MPRBRAIN CO.LTD]1Legacy NDC, 1 package rows20201023_b2405198-d162-ce66-e053-2995a90a6d0a.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74741-117074741-1170-1

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
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b24051aa-2908-97eb-e053-2a95a90a2150b2405198-d162-ce66-e053-2995a90a6d0a2020-10-22Exact identifier
spl id: b24051aa-2908-97eb-e053-2a95a90a2150
spl set id: b2405198-d162-ce66-e053-2995a90a6d0a

Reported adverse events (FAERS/openFDA)#

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