NDC 72802-001 Be The Skin Natural Base Sun

NDC Product Code 72802-001

NDC CODE: 72802-001

Proprietary Name: Be The Skin Natural Base Sun What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

  • 72802 - Betheskin Co.,ltd

NDC 72802-001-02

Package Description: 1 CONTAINER in 1 CARTON > 50 g in 1 CONTAINER (72802-001-01)

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

NDC Product Information

Be The Skin Natural Base Sun with NDC 72802-001 is a product labeled by Betheskin Co.,ltd. The product's dosage form is and is administered via form.

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.

  • MAGNOLIA LILIIFLORA WHOLE (UNII: GDO2997SZZ)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • WATER (UNII: 059QF0KO0R)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • BEMOTRIZINOL (UNII: PWZ1720CBH)
  • AMILOXATE (UNII: 376KTP06K8)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
  • PAEONIA X SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J)
  • GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
  • SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
  • CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
  • CYCLOMETHICONE (UNII: NMQ347994Z)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • ALUMINUM STEARATE (UNII: U6XF9NP8HM)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
  • GLYCERYL BEHENATE/EICOSADIOATE (UNII: 73CJJ317SR)
  • HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)
  • HYDRATED SILICA (UNII: Y6O7T4G8P9)
  • ROYAL JELLY (UNII: L497I37F0C)
  • MICA (UNII: V8A1AW0880)
  • STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: 657L0NC5MT)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)

Product Labeler Information

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

Labeler Name: Betheskin Co.,ltd
Labeler Code: 72802
Start Marketing Date: 02-12-2019 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: 12-31-2020 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 - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Be The Skin Natural Base Sun Product Label Images

Be The Skin Natural Base Sun 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

Octinoxate 7.00%


Titanium Dioxide 5.30%


Zinc Oxide 3.90%

Otc - Purpose

Sunscreen

Indications & Usage

Helps prevent sunburn

Dosage & Administration

Apply liberally 15 minutes before sun exposure. Reapply at least every two hours

Warnings

For external use only.


Do not use on damaged or broken skin.


When using this product, keep out of eyes. Rinse with water to remove.


Stop using and ask a doctor if rash occurs.

Otc - Keep Out Of Reach Of Children

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

Inactive Ingredient

Magnolia Liliflora Bud Extract, Cyclopentasiloxane, Water, Butylene Glycol, C12-15 Alkyl Benzoate, Isoamyl p-Methoxycinnamate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Disteardimonium Hectorite, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Glyceryl Behenate/Eicosadioate, Sodium Chloride, Triethoxycaprylylsilane, Mica, Methyl Methacrylate Crosspolymer, Cyclomethicone, Hydrogen Dimethicone, Hydrated Silica, Aluminum Hydroxide, Propylene Glycol Isostearate, Aluminum Stearate, Polyhydroxystearic Acid, Alumina, Scutellaria Baicalensis Root Extract, Paeonia Suffruticosa Root Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Laurus Nobilis Leaf Extract, Artemisia Umbelliformis Extract, Buddleja Davidii Extract, Thymus Vulgaris (Thyme) Flower/Leaf Extract, Aloe Barbadensis Leaf Extract, Honey Extract, Royal Jelly Extract, Tocopheryl Acetate, Stearyl Glycyrrhetinate, Disodium EDTA, Iron Oxides (CI 77491), Iron Oxides (CI 77492), Iron Oxides (CI 77499), Fragrance

* Please review the disclaimer below.