FDA.reportPublic FDA data

Club Amucheer Quick Water In Foundation Natural Beige

Manufacturer
Club Cosmetics Co., Ltd.
Effective date
2020-11-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:08:31

Label at a glance#

ProductClub Amucheer Quick Water In Foundation Natural Beige
Active ingredientTITANIUM DIOXIDE
Label structure6 sections

Dosage and administration

Directions Apply thin layer over clean face as needed apply liberally before sun exposure and as needed children under 6 months of age: ask a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 13.89%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Warnings

WARNINGS SECTION

Warnings

For external use only

When using this product

  • keep out of the eye area
  • rinse with water to remove

Stop use and ask a doctor if rash or irritation occurs or lasts

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

Apply thin layer over clean face as needed

  • apply liberally before sun exposure and as needed
  • children under 6 months of age: ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

talc, silica, nylon-12, diisostearyl malate, squalane, zinc myristate, dimethicone, pentylene glycol, methicone, dimethicone/vinyl dimethicone crosspolymer, hydrogen dimethicone, hydrated silica, phenoxyethanol, hydroxyapatite, fragrance, tocopherol, lauroyl lysine, sodium hyaluronate, mica, aluminum hydroxide, iron oxides

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Club Amucheer QWI Foundation NBClub Amucheer QWI Foundation NB

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80999-001180999-0011-1

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
DIISOSTEARYL MALATEQBS8A3XZGQIACT
TALC7SEV7J4R1UIACT
SQUALANEGW89575KF9IACT
NYLON-12446U8J075BIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
c5764aeb-5fb0-2f56-e053-2a95a90a458ab38112ab-e515-e0ed-e053-2995a90a4b5f2021-06-23WarningsExact identifier
spl set id: b38112ab-e515-e0ed-e053-2995a90a4b5f

Reported adverse events (FAERS/openFDA)#

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