FDA.reportPublic FDA data

Crepe Corrector Booy

Manufacturer
Yiwu Yucheng E Commerce Co Ltd
Effective date
2024-11-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:38:57

Label at a glance#

ProductCrepe Corrector Booy
Active ingredientNIACINAMIDE
Label structure11 sections

Label contents#

Full prescribing information#

COMPONENTS

Salicylic acid 2%

OTC - PURPOSE SECTION

wart remover

INDICATIONS & USAGE SECTION

Apply twice daly(moring and night as a man and once as a woman.Afer apicaion, proeed with an acive masage for 3-5 minutes unthe product is fuy absorbed

WARNINGS SECTION

Forevemaluseony Avoid coniac wth eves li coniac ocus nse ihorouthly wt waier Keep out ofreach oi chidrenifvou ale preanant.nursing. otiaveanyunderving medca condion.consutyou healthcare provider before using the product

DOSAGE & ADMINISTRATION SECTION

For external use only.

OTC - DO NOT USE SECTION

Discontinue use if any irritation or adverse reaction occurs

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. lf contact occurs, rinse thoroughly with waterDiscontinue use if any irritation or adverse reaction occurs.

OTC - STOP USE SECTION

on broken or irritated scalp

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If sxralowed, get medical help or contact a Poison Conirol Cenler ngiht away.

INACTIVE INGREDIENT SECTION

Acrylates copolymer, Ethyl acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84756-406-012024-12-23C16284748780-129f3f9da-5c5f-8323-e063-dbdaa90a1b67277b0972-ddbf-e868-e063-6394a90a1e74
84756-406-022024-12-23C16284748780-129f3f9da-5c5f-8323-e063-dbdaa90a1b67277b0972-ddbf-e868-e063-6394a90a1e74
84756-406-032024-12-23C16284748780-129f3f9da-5c5f-8323-e063-dbdaa90a1b67277b0972-ddbf-e868-e063-6394a90a1e74
84756-406-042024-12-23C16284748780-129f3f9da-5c5f-8323-e063-dbdaa90a1b67277b0972-ddbf-e868-e063-6394a90a1e74
84756-406-052024-12-23C16284748780-129f3f9da-5c5f-8323-e063-dbdaa90a1b67277b0972-ddbf-e868-e063-6394a90a1e74

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84756-406-01Crepe Corrector Booy5 g in 1 BOXCREAM51
84756-406-02Crepe Corrector Booy15 g in 1 BOXCREAM151
84756-406-03Crepe Corrector Booy30 g in 1 BOXCREAM301
84756-406-04Crepe Corrector Booy50 g in 1 BOXCREAM501
84756-406-05Crepe Corrector Booy100 g in 1 BOXCREAM1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84756-406CREPE CORRECTOR BOOY CREAM [YIWU YUCHENG E COMMERCE CO LTD]15 package rows20241126_277b0972-ddbf-e868-e063-6394a90a1e74.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
84756-40684756-406-01, 84756-406-02, 84756-406-03, 84756-406-04, 84756-406-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
SESAME OILQX10HYY4QVIACT
CHLORPHENESINI670DAL4SZIACT
PALMITOYL PENTAPEPTIDE-4KK181SM5JGIACT
NIACINAMIDE25X51I8RD4ACTIB
PALMITOYL TRIPEPTIDE-1RV743D216MIACT

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
277b0972-ddc0-e868-e063-6394a90a1e74277b0972-ddbf-e868-e063-6394a90a1e742024-11-22WarningsExact identifier
spl id: 277b0972-ddc0-e868-e063-6394a90a1e74
spl set id: 277b0972-ddbf-e868-e063-6394a90a1e74

Reported adverse events (FAERS/openFDA)#

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