FDA.reportPublic FDA data

Licorice Root Whitening cream

Manufacturer
Yiwu Xinqian E Commerce Co Ltd
Effective date
2024-11-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:38:56

Label at a glance#

ProductLicorice Root Whitening cream
Active ingredientNIACINAMIDE
Label structure10 sections

Label contents#

Full prescribing information#

COMPONENTS

Salicylic acid 2%

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
84756-436-012024-12-23C16284748780-129f3f9da-5ac4-8323-e063-dbdaa90a1b6727a2a2fa-29fd-06bf-e063-6394a90ae353
84756-436-022024-12-23C16284748780-129f3f9da-5ac4-8323-e063-dbdaa90a1b6727a2a2fa-29fd-06bf-e063-6394a90ae353
84756-436-032024-12-23C16284748780-129f3f9da-5ac4-8323-e063-dbdaa90a1b6727a2a2fa-29fd-06bf-e063-6394a90ae353
84756-436-042024-12-23C16284748780-129f3f9da-5ac4-8323-e063-dbdaa90a1b6727a2a2fa-29fd-06bf-e063-6394a90ae353
84756-436-052024-12-23C16284748780-129f3f9da-5ac4-8323-e063-dbdaa90a1b6727a2a2fa-29fd-06bf-e063-6394a90ae353

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84756-436-01Licorice Root Whitening cream5 g in 1 BOXCREAM51
84756-436-02Licorice Root Whitening cream15 g in 1 BOXCREAM151
84756-436-03Licorice Root Whitening cream30 g in 1 BOXCREAM301
84756-436-04Licorice Root Whitening cream50 g in 1 BOXCREAM501
84756-436-05Licorice Root Whitening cream100 g in 1 BOXCREAM1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84756-436LICORICE ROOT WHITENING CREAM CREAM [YIWU XINQIAN E COMMERCE CO LTD]15 package rows20241125_27a2a2fa-29fd-06bf-e063-6394a90ae353.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
84756-43684756-436-01, 84756-436-02, 84756-436-03, 84756-436-04, 84756-436-05

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
CHLORPHENESINI670DAL4SZIACT
SESAME OILQX10HYY4QVIACT
GLYCERINPDC6A3C0OXIACT
NIACINAMIDE25X51I8RD4ACTIB
PALMITOYL PENTAPEPTIDE-4KK181SM5JGIACT
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
27a2a2fa-29fe-06bf-e063-6394a90ae35327a2a2fa-29fd-06bf-e063-6394a90ae3532024-11-24WarningsExact identifier
spl id: 27a2a2fa-29fe-06bf-e063-6394a90ae353
spl set id: 27a2a2fa-29fd-06bf-e063-6394a90ae353

Reported adverse events (FAERS/openFDA)#

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