FDA.reportPublic FDA data

Note BB Concealer 01

Manufacturer
ALTONA COSMETICS TECHNOLOGY SANAYI VE TICARET ANONIM SIRKETI
Effective date
2024-09-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:19:38

Label at a glance#

ProductNote BB Concealer 01
Active ingredientOCTINOXATE
Label structure7 sections

Indications and uses

helps prevent sunburn if used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

Apply liberally 15 minutes before sun exposure Reapply at least every 2 hours Use a water resistant sunscreen if swimming or sweating Sun Protection Measures.  Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 0.6%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15 minutes before sun exposure
  • Reapply at least every 2 hours
  • Use a water resistant sunscreen if swimming or sweating
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • limit time in the sun, especially from 10 a.m.-2 p.m.
  • wear long-sleeved shirts, pants, hats, and sunglasses
  • Children under 6 months of age: Ask a doctor

Other information

SPL UNCLASSIFIED SECTION

  • Protect the product in this container from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Water (Aqua), PEG-10 Dimethicone, Butylene Glycol, Dimethicone, HDI/Trimethylol Hexyllactone Crosspolymer, Disteardimonium Hectorite, Aluminum Starch Octenylsuccinate, Phenoxyethanol, Alcohol, Triethoxycaprylylsilane, Glycerin, Tocopheryl Acetate, Trimethylsiloxysilicate, Bran (Triticum vulgare) Extract, Sodium Chloride, Dimethicone/Vinyl Dimethicone Crosspolymer, Propylene Glycol, Ethylhexylglycerin, Silica, BHT, Bitter Orange(Citrus aurantium) Fruit Extract, Grapefruit (Citrus paradisi) Fruit Extract, Lecithin, Sorbitol, Sodium Ascorbate, Sunflower (Helianthus annus) Seed Oil, Tocopherol, Sodium Hydroxide. May contain: Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, CI 77492, CI 77499)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Label1Outer Label1inner Label1inner Label1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70474-015-012025-11-26C16284748780-13b156c62-348c-fb37-e063-e6dba90a4e07Note BB Concealer Sunscreen SPF 15, 01
70474-015-012025-07-29C16284748780-13b156c62-348c-fb37-e063-e6dba90a4e07Note BB Concealer Sunscreen SPF 15, 01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70474-015-01Note BB Concealer 0110 mL in 1 TUBECREAM101
70474-015-01Note BB Concealer 011 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70474-015NOTE BB CONCEALER 01 (OCTINOXATE) CREAM [ALTONA COSMETICS TECHNOLOGY SANAYI VE TICARET ANONIM SIRKETI]1Current NDC, 2 package rows20240918_7ea1a3f4-4f99-4cb4-bbd5-112428903731.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70474-01570474-015-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
GRAPEFRUITO82C39RR8CIACT
WHEAT4J2I0SN84YIACT
CYCLOMETHICONE 50THT5PCI0RIACT
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
DIMETHICONE, UNSPECIFIED92RU3N3Y1OIACT
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMERWB5K9Y35Y9IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALCOHOL3K9958V90MIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
SODIUM CHLORIDE451W47IQ8XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
BITTER ORANGEDQD16J2B5OIACT
SORBITOL506T60A25RIACT
SODIUM ASCORBATES033EH8359IACT
SUNFLOWER OIL3W1JG795YIIACT
TOCOPHEROLR0ZB2556P8IACT
SODIUM HYDROXIDE55X04QC32IIACT
OCTINOXATE4Y5P7MUD51ACTIB

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
Note BB Concealer 01OCTINOXATEALTONA COSMETICS TECHNOLOGY SANAYI VE TICARET ANONIM SIRKETI7ea1a3f4-4f99-4cb4-bbd5-1124289037312024-09-16WarningsExact identifier
ndc (package): 70474-015-01
ndc (product): 70474-015
ndc11 (package): 70474001501
spl id: 223e8437-178d-9ab3-e063-6394a90a0267
spl set id: 7ea1a3f4-4f99-4cb4-bbd5-112428903731

Reported adverse events (FAERS/openFDA)#

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