NDC 70550-000 Recapture Day Plus Ir Defense

NDC Product Code 70550-000

NDC CODE: 70550-000

Proprietary Name: Recapture Day Plus Ir Defense 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

NDC 70550-000-07

Package Description: 1 JAR in 1 CARTON > 50 mL in 1 JAR

NDC 70550-000-68

Package Description: 1 JAR in 1 CARTON > 30 mL in 1 JAR

NDC 70550-000-83

Package Description: 1 JAR in 1 CARTON > 15 mL in 1 JAR

NDC 70550-000-98

Package Description: 1 JAR in 1 CARTON > 30 mL in 1 JAR

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

NDC Product Information

Recapture Day Plus Ir Defense with NDC 70550-000 is a product labeled by Atlantic Coast Media Group, Llc.. 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.

  • ISODODECANE (UNII: A8289P68Y2)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
  • XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
  • DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • PHORMIDIUM PERSICINUM (UNII: ZA983U4810)
  • LAMINARIA DIGITATA (UNII: 15E7C67EE8)
  • POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
  • SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
  • BAKUCHIOL (UNII: OT12HJU3AR)
  • AMINOPROPYL ASCORBYL PHOSPHATE (UNII: 290O2PQ83R)
  • SOYBEAN OIL (UNII: 241ATL177A)
  • ERGOTHIONEINE (UNII: BDZ3DQM98W)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • SHEA BUTTER (UNII: K49155WL9Y)
  • CHICORY ROOT (UNII: 090CTY533N)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0)
  • CHINESE CINNAMON (UNII: WS4CQ062KM)
  • JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432)
  • APRICOT (UNII: 269CJD5GZ9)
  • APPLE (UNII: B423VGH5S9)
  • CLOVE (UNII: K48IKT5321)
  • CANTALOUPE (UNII: 8QF5D5H6UH)
  • ORCHIS MASCULA FLOWER (UNII: 6H1JQK35LA)
  • CANANGA ODORATA FLOWER (UNII: 76GTF6Z97M)
  • OCTADECANE (UNII: N102P6HAIU)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • STEARYL DIMETHICONE (400 MPA.S AT 50C) (UNII: R327X197HY)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • ANHYDROXYLITOL (UNII: 8XWR7NN42F)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • COCO GLUCOSIDE (UNII: ICS790225B)
  • XYLITOL (UNII: VCQ006KQ1E)
  • DIMETHICONE/BIS-ISOBUTYL PPG-20 CROSSPOLYMER (UNII: O4I3UFO6ZF)
  • SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • MICA (UNII: V8A1AW0880)
  • STANNIC OXIDE (UNII: KM7N50LOS6)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Labeler Information

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

Labeler Name: Atlantic Coast Media Group, Llc.
Labeler Code: 70550
Start Marketing Date: 03-01-2015 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: 12-31-2018 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 - 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.

Recapture Day Plus Ir Defense Product Label Images

Recapture Day Plus Ir Defense 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

DISTRIBUTED BY:Christie Brinkley Skincare, LLC


Jersey City, NJ 07310

Otc - Purpose

Active ingredientsPurposeAvobenzone 3.0%SunscreenOctinoxate 7.5%SunscreenOctocrylene 4.2%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 - Stop Use

Stop use and ask a doctor if rash occurs.

Otc - When Using

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

Otc - Keep Out Of Reach Of Children

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

Directions

  • 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 doctorSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease 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 sunglasses

Other Information

  • Protect this product from excessive heat and direct sunlightYou may report a serious adverse reaction from using this product to Report Reaction, LLC. PO Box 22, Plainsboro, NJ 08536-0222

Inactive Ingredients

Water, Isododecane, Cyclopentasiloxane, Butylene Glycol, Glycerin, Cetyl Alcohol, Sodium Potassium Aluminum Silicate, Ethylhexyl Methoxycrylene, Xylitylglucoside, Diethylhexyl Syringylidenemalonate, Glyceryl Stearate, PEG-100 Stearate, Phormidium Persicinum Extract, Laminaria Digitata Extract, Polygonum Aviculare Extract, Methylglucoside Phosphate, Copper Lysinate/Prolinate, Simmondsia Chinensis (Jojoba) Seed Extract, Bakuchiol, Aminopropyl Ascorbyl Phosphate, Glycine Soja (Soybean) Oil, Ergothioneine, Tocopheryl Acetate, Rose Extract, Butyrospermum Parkii (Shea) Butter, Cichorium Intybus (Chicory) Root Extract, Camellia Sinensis Leaf Extract, Cinnamomum Cassia Bark Extract, Coffea Arabica (Coffee) Leaf/Seed Extract, Jasminum Officinale (Jasmine) Flower/Leaf Extract, Prunus Armeniaca (Apricot) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Eugenia Caryophyllus (Clove) Flower Extract, Cucumis Melo Cantalupensis Fruit Extract, Orchis Mascula Flower Extract, Cananga Odorata Flower Extract, Octadecane, Sea Water, Stearyl Dimethicone, Silica, Anhydroxylitol, Cetearyl Alcohol, Carbomer, Ethylhexylglycerin, Aminomethyl Propanol, Coco-Glucoside, Xylitol, Dimethicone/Bis-Isobutyl PPG-20 Crosspolymer, Sodium Dehydroacetate, Caprylic/Capric Triglyceride, Disodium EDTA, Phenoxyethanol, Chlorphenesin, Benzyl Alcohol, Mica, Tin Oxide, Titanium Dioxide

* Please review the disclaimer below.