NDC 58544-001 All Aglow Perfect Cushion Foundation

NDC Product Code 58544-001

NDC 58544-001-01

Package Description: 15 mL in 1 BOTTLE, GLASS

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

All Aglow Perfect Cushion Foundation with NDC 58544-001 is a product labeled by Hankook Cosmetics Manufacturing Co., Ltd._eumseong Factory. The generic name of All Aglow Perfect Cushion Foundation is . The product's dosage form is and is administered via form.

Labeler Name: Hankook Cosmetics Manufacturing Co., Ltd._eumseong Factory

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • PEG-80 STEARATE (UNII: 1X2OAT3BFK)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)
  • CITRUS MEDICA FRUIT (UNII: ZE5Q6PN9ON)
  • ALUMINUM HYDROXIDE SULFATE (AL(OH)(SO4)) (UNII: 9QO62ZS7VO)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • NIACINAMIDE (UNII: 25X51I8RD4)
  • CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
  • TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
  • PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
  • PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • BENTOQUATAM (UNII: 7F465U79Q1)
  • STEARYL CAPRYLATE (UNII: 06TS6O9194)
  • POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
  • BROWN IRON OXIDE (UNII: 1N032N7MFO)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • BORON NITRIDE (UNII: 2U4T60A6YD)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • CHOLESTEROL (UNII: 97C5T2UQ7J)
  • CITRUS MAXIMA FRUIT RIND OIL (UNII: 8U3877WD44)
  • ORANGE OIL (UNII: AKN3KSD11B)
  • ROSEMARY OIL (UNII: 8LGU7VM393)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)
  • HONEY (UNII: Y9H1V576FH)
  • JUNIPERUS DEPPEANA WOOD OIL (UNII: 4739QA5686)
  • ADENOSINE (UNII: K72T3FS567)
  • NEPIDERMIN (UNII: TZK30RF92W)
  • BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)
  • MECASERMIN (UNII: 7GR9I2683O)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Hankook Cosmetics Manufacturing Co., Ltd._eumseong Factory
Labeler Code: 58544
Start Marketing Date: 08-25-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

All Aglow Perfect Cushion Foundation Product Label Images

All Aglow Perfect Cushion Foundation Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Titanium Dioxide 9%Octyl methoxycinnamate 7%Octyl Salicylate 4.8%Octocrylene 2%Zinc Oxide 2%

Indications & Usage

USESHelps 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

– For External use only.

– Keep out of eyes. Rinse with water to remove.

– Stop use if a rash develops. Consult a physician.

.

Directions

Apply liberally 15 minutes before sun exposure.

Reapply at least every 2 hours.

Other Information

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

Inactive Ingredients

WATER, CYCLOPENTASILOXANE (CYCLOMETHICONE), DIPHENYLSILOXY

PHENYL TRIMETHICONE, CYCLOHEXASILOXANE (CYCLOMETHICONE),

C12-15 ALKYL BENZOATE, NIACINAMIDE, CAPRYLYL METHICONE,

TRIMETHYLSILOXYSILICATE, PEG-30 DIPOLYHYDROXYSTEARATE,

PEG-10 DIMETHICONE, BUTYLENE GLYCOL, VINYL

DIMETHICONE/METHICONE SILSESQUIOXANE CRTOSSPOLYMER,

SODIUM CHLORIDE, QUATERNIUM-18 BENTONITE,

ACRYLATES/STEARYL ACRYLATE/DIMETHICONE METHACRYLATE

COPOLYMER, POLYMETHYL METHACRYLATE, IRON OXIDE,

DIMETHICONE, ACRYLATES/DIMETHICONE COPOLYMER, BORON

NITRIDE, CHLORPHENESIN, TRIETHOXYCAPRYLYLSILANE,

ALUMINA (CI 77002), CITRUS MEDICA LIMONUM (LEMON) PEEL

OIL, ADENOSINE, HONEY, LAVANDULA ANGUSTIFOLIA (LAVENDER)

OIL, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL,

EUCALYPTUS GLOBULUS LEAF OIL, CITRUS AURANTIUM DULCIS

(ORANGE) PEEL OIL, CITRUS GRANDIS (GRAPEFRUIT) PEEL OIL,

HYDROGENATED LECITHIN, 1,2-HEXANEDIOL, CHOLESTEROL,

PEG-800, GLYCERIN, POLYSORBATE 20, SH-OLIGOPEPTIDE-1,

SH-POLYPEPTIDE-1, SH-POLYPEPTIDE-8, SH-POLYPEPTIDE-9,

SH-POLYPEPTIDE-45, SH-OLIGOPEPTIDE-2, SH-POLYPEPTIDE-22.

Otc - Purpose

PURPOSE SUNSCREEN

Otc - Keep Out Of Reach Of Children

Keep out of reach of childrenIf product is swallowed, get medical help or contact a poison control center right away

* Please review the disclaimer below.