NDC 58411-260 Shiseido Ultimate Sun Protection S

NDC Product Code 58411-260

NDC 58411-260-10

Package Description: 1 BOTTLE in 1 CARTON > 100 mL in 1 BOTTLE

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

NDC Product Information

Shiseido Ultimate Sun Protection S with NDC 58411-260 is a product labeled by Shiseido Americas Corporation. The generic name of Shiseido Ultimate Sun Protection S is . The product's dosage form is and is administered via form.

Labeler Name: Shiseido Americas Corporation

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.

  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • WATER (UNII: 059QF0KO0R)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
  • POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
  • HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
  • PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
  • CYCLOMETHICONE (UNII: NMQ347994Z)
  • PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)
  • POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
  • TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
  • POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
  • PEG/PPG-14/7 DIMETHYL ETHER (UNII: 6DNW9T7YT2)
  • SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
  • RASPBERRY (UNII: 4N14V5R27W)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • THYMUS SERPYLLUM (UNII: 86H4S6K51N)
  • ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • ISOSTEARIC ACID (UNII: X33R8U0062)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • HYDRATED SILICA (UNII: Y6O7T4G8P9)
  • SODIUM METAPHOSPHATE (UNII: 532IUT7IRV)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
  • .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
  • SYZYGIUM JAMBOS LEAF (UNII: 407Z4W5LFF)

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: 02-01-2016 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: 12-31-2020 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 Ultimate Sun Protection S Product Label Images

Shiseido Ultimate Sun Protection S 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

Otc - Purpose

Active ingredientsPurposeTITANIUM DIOXIDE 9.1%SunscreenZINC OXIDE 19.3%Sunscreen

Uses

  • Helps prevent sunburnif 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

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 exposurereapply:after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hoursSun 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 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-sleeve shirts, pants, hats, and sunglasseschildren under 6 months: Ask a doctor

Inactive Ingredients

DIMETHICONE • WATER • BUTYLENE GLYCOL • GLYCERIN • DIISOPROPYL SEBACATE • POLYMETHYL METHACRYLATE • HYDROGENATED POLYDECENE • PEG-10 DIMETHICONE • CYCLOMETHICONE • PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE • BIS-BUTYLDIMETHICONE POLYGLYCERYL-3 • PEG-6 • TRIMETHYLSILOXYSILICATE • PEG-32 • PEG/PPG-14/7 DIMETHYL ETHER • SCUTELLARIA BAICALENSIS ROOT EXTRACT • RUBUS IDAEUS (RASPBERRY) FRUIT EXTRACT • ALOE BARBADENSIS LEAF EXTRACT • THYMUS SERPILLUM EXTRACT • ALUMINUM DISTEARATE • ALUMINUM HYDROXIDE • HYDROGEN DIMETHICONE • ISOSTEARIC ACID • DISTEARDIMONIUM HECTORITE • HYDRATED SILICA • SODIUM METAPHOSPHATE • TRIETHOXYCAPRYLYLSILANE • STEARIC ACID • DEXTRIN PALMITATE • DISTEARYLDIMONIUM CHLORIDE • TOCOPHEROL • SYZYGIUM JAMBOS LEAF EXTRACT •

Other Information

  • Protect this product in this container from excessive heat and direct sun.avoid contact with clothing and other textiles-may stain.

* Please review the disclaimer below.