FDA.reportPublic FDA data

ANYIBEAUTY FACE

Manufacturer
Guangzhou Zhicunxiu Cosmetics Co., Ltd
Effective date
2023-12-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:18:12

Label at a glance#

ProductANYIBEAUTY FACE
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

treats and helps prevent acne

Dosage and administration

Lather onto wet skin and massage for 12 minutes. Rinse throughly For best result, use it regularly.

Storage and handling

store in a cool dry place, away from direct sunlight.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 0.5%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Uses

INDICATIONS & USAGE SECTION

treats and helps prevent acne

Warnings

WARNINGS SECTION

For external use only.Avoid direct contact with eyes.

Do not use on open wounds, eczema and dermatitis.
Stop using if red spots, swelling, itching or irritation occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

lf pregnant or breast-feeding, ask a healthcare professional before use. lf accidental ingestion and adverse reaction occurs, get medical help or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Lather onto wet skin and massage for 12 minutes.
  • Rinse throughly For best result, use it regularly.

Other Information

STORAGE AND HANDLING SECTION

store in a cool dry place, away from direct sunlight.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium Palmate, Sodium Palm Kernelate, Calcium Carbonate, Curcuma Longa Root, Propolis Extract, Hydrogenated Olive Oil, Tocopherylacetate, Aqua, Cocamidopropyl Betaine, Disodium EDTA, BHT, Disodium Distvrylbiphenyl Disulfonate, CI 19140, CI 16255, CI 15985, CI 16185, Parfum

Questions?

OTC - QUESTIONS SECTION

Email-us zcunxiu@163.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel83867-0013-183867-0013-183867-0013-283867-0013-283867-0013-383867-0013-383867-0013-483867-0013-4

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
83867-001383867-0013-1, 83867-0013-2, 83867-0013-3, 83867-0013-4

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
SALICYLIC ACIDO414PZ4LPZACTIB
CALCIUM CARBONATEH0G9379FGKIACT
SODIUM PALMATES0A6004K3ZIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM PALM KERNELATE6H91L1NXTWIACT
WATER059QF0KO0RIACT

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
0c73ebe2-c585-cac0-e063-6294a90a01f40c52d11a-e29b-11fe-e063-6294a90a90782023-12-14WarningsExact identifier
spl id: 0c73ebe2-c585-cac0-e063-6294a90a01f4
spl set id: 0c52d11a-e29b-11fe-e063-6294a90a9078

Reported adverse events (FAERS/openFDA)#

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