NDC 58411-257 Shiseido Protective Lip Conditioner

  1. Labeler Index
  2. Shiseido Americas Corporation
  3. NDC: 58411-257 Shiseido Protective Lip Conditioner

NDC Product Code 58411-257

NDC CODE: 58411-257

Proprietary Name: Shiseido Protective Lip Conditioner 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This product is used as sunscreen

NDC Code Structure

NDC 58411-257-20

Package Description: 1 CARTRIDGE in 1 CARTON > 4 g in 1 CARTRIDGE

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

NDC Product Information

Shiseido Protective Lip Conditioner with NDC 58411-257 is product labeled by Shiseido Americas Corporation. 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.
  • POLYGLYCERYL-2 TRIISOSTEARATE (UNII: 68DUY2D39A)
  • TRIISOSTEARIN (UNII: 71503RH8KG)
  • MACADAMIA OIL (UNII: 515610SU8C)
  • HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
  • DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)
  • TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
  • MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
  • CANDELILLA WAX (UNII: WL0328HX19)
  • MICA (UNII: V8A1AW0880)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • WATER (UNII: 059QF0KO0R)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • ARGININE HYDROCHLORIDE (UNII: F7LTH1E20Y)
  • PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
  • XYLITOL (UNII: VCQ006KQ1E)
  • .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
  • .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • FERROSOFERRIC OXIDE (UNII: XM0M87F357)
  • ALLANTOIN (UNII: 344S277G0Z)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • TRIMETHYLOLPROPANE TRIETHYLHEXANOATE (UNII: B952ZGW1IL)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • METHICONE (20 CST) (UNII: 6777U11MKT)
  • TETRADECENE (UNII: FW23481S7S)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)

Product Labeler Information

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

Labeler Name: Shiseido Americas Corporation
Labeler Code: 58411
Start Marketing Date: 09-01-2015 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.

Shiseido Protective Lip Conditioner Product Label Images

Shiseido Protective Lip Conditioner 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

Other

Drug Facts

Active Ingredients

OCTINOXATE 4.9%

Purpose

Sunscreen

Uses

  • Helps prevent sunburn

Skin Cancer/Skin Aging Alert

Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging.For external use only

Otc - Do Not Use

Do not use on damaged or broken skin

Otc - When Using

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

Otc - Stop Use

Stop use and ask a doctor if rash occurs

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • For sunscreen use:apply liberally 15 minutes before sun exposureuse a water resistant sunscreen if swimming or sweatingreapply at least every 2 hourschildren under 6 months: Ask a doctor

Inactive Ingredients

POLYGLYCERYL-2 TRIISOSTEARATE•TRIISOSTEARIN•MACADAMIA TERNIFOLIA SEED OIL•POLYETHYLENE•DIPHENYLSILOXY PHENYL TRIMETHICONE•TRIETHYLHEXANOIN•MICROCRYSTALLINE WAX•EUPHORBIA CERIFERA (CANDELILLA) WAX•SODIUM MAGNESIUM SILICATE•GLYCERIN•WATER•ARGININE HCl•XYLITOL•TOCOPHERYL ACETATE•ALLANTOIN•SODIUM HYALURONATE•PEG-10 DIMETHICONE•TOCOPHEROL•SIMETHICONE•BHT•TRIMETHYLOLPROPANE TRIETHYLHEXANOATE•METHICONE•TETRADECENE•SILICA•ALUMINUM HYDROXIDE•POLYSILICONE-2•FRAGRANCE•MICA•TITANIUM DIOXIDE•IRON OXIDES•

Other Information

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

* Please review the disclaimer below.