FDA.reportPublic FDA data

BANSBAO SKIN BRIGHTENING & SPOTS-REMOVING CREAM

Manufacturer
Mengfei Li Inc.
Effective date
2019-04-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:59:14

Label at a glance#

ProductBANSBAO SKIN BRIGHTENING AND SPOTS-REMOVING
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

For brightening, removing acne, and spots.

Storage and handling

Store at room temperature

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Uses

INDICATIONS & USAGE SECTION

For brightening, removing acne, and spots.

Warnings

WARNINGS SECTION

  • For external use only.
  • When using this product. skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time, if irritation occurs, use only one topical acne medication at a time, Avoid contact with eyes. If contact occurs, flush thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact poison control center right away.

Direction. Cleanse twice a day

DOSAGE & ADMINISTRATION SECTION

  • Wet face. Apply to hands, add water and work into a lather.
  • Massage face gently.

Other Information:

STORAGE AND HANDLING SECTION

Store at room temperature

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water, glycerin, propylene glycol, squalane, dimethicone, cyclomethicone, hydroxyethyl urea, glycine, ammonium polyacryloyldimethyl taurate, tocopherol, glucose, mannose, polyglucuronic acid, sodium hyaluronate, Prunus persica (peach) flower extract, Nelumbo nucifera flower extract, Hibiscus militaris flower extract, methylparaben, caprylhydroxamic acid, glyceryl caprylate, disodium EDTA, fragrance.

SPL UNCLASSIFIED SECTION

Bansbao

PRO-CARE

A medicated cream for brightening, removing acne, and spots.

Made in USA

U.S. Distributor:

Mengfei Li Inc. DBA Bansbao USA

Arcadia, CA 91007

www.bansbaousa.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
cb89b86a-369e-4204-8910-ae797c503af3Product name120230706
d4880ace-a516-8c47-8dfd-73a4ba5887d7Product name220180830
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72889-526-952020-09-27C16284748780-1ab0e2407-2ed3-f274-e053-dbdaa90a6471BANSBAO SKIN BRIGHTENING & SPOTS-REMOVING CREAM
72889-526-952020-09-25C16284748780-1ab0e2407-2ed3-f274-e053-dbdaa90a6471BANSBAO SKIN BRIGHTENING & SPOTS-REMOVING CREAM
72889-526-952020-07-22C16284748780-1ab0e2407-2ed3-f274-e053-dbdaa90a6471BANSBAO SKIN BRIGHTENING & SPOTS-REMOVING CREAM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72889-526-95BANSBAO SKIN BRIGHTENING AND SPOTS-REMOVING1 in 1 BOXCREAM11
72889-526-95BANSBAO SKIN BRIGHTENING AND SPOTS-REMOVING50 g in 1 BOTTLECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72889-526BANSBAO SKIN BRIGHTENING AND SPOTS-REMOVING (SALICYLIC ACID) CREAM [MENGFEI LI INC.]1Legacy NDC, 2 package rows20190417_bc765a0f-a747-48c7-9ed3-fac96fbc8433.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72889-52672889-526-95

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SQUALANEGW89575KF9IACT
DIMETHICONE92RU3N3Y1OIACT
CYCLOMETHICONENMQ347994ZIACT
HYDROXYETHYL UREAMBQ7DDQ7ARIACT
GLYCINETE7660XO1CIACT
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S)F01RIY4371IACT
TOCOPHEROLR0ZB2556P8IACT
ANHYDROUS DEXTROSE5SL0G7R0OKIACT
MANNOSE, L-2W3YE50TX8IACT
POLYGALACTURONIC ACIDVV3XD4CL04IACT
HYALURONATE SODIUMYSE9PPT4THIACT
PRUNUS PERSICA FLOWER19GWB0JENHIACT
NELUMBO NUCIFERA FLOWER61W322NLDVIACT
HIBISCUS LAEVIS FLOWER10813RME15IACT
METHYLPARABENA2I8C7HI9TIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
GLYCERYL MONOCAPRYLATETM2TZD4G4AIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
FAGRAEA BERTEROANA FLOWER OIL6665W245VPIACT

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
f2b982cb-0eab-453f-85bf-5abf5230a7c8bc765a0f-a747-48c7-9ed3-fac96fbc84332019-04-04WarningsExact identifier
spl id: f2b982cb-0eab-453f-85bf-5abf5230a7c8
spl set id: bc765a0f-a747-48c7-9ed3-fac96fbc8433

Reported adverse events (FAERS/openFDA)#

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