NDC 71876-003 Prescribers Choice Dynamic Broad Spectrum

NDC Product Code 71876-003

NDC CODE: 71876-003

Proprietary Name: Prescribers Choice Dynamic Broad Spectrum 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

  • 71876 - Prescriber's Choice Inc.
    • 71876-003 - Prescribers Choice Dynamic Broad Spectrum

NDC 71876-003-50

Package Description: 50 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

Prescribers Choice Dynamic Broad Spectrum with NDC 71876-003 is a product labeled by Prescriber's Choice Inc.. 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.

  • WATER (UNII: 059QF0KO0R)
  • OCTYL STEARATE (UNII: 772Y4UFC8B)
  • POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
  • CYCLOMETHICONE (UNII: NMQ347994Z)
  • SUNFLOWER OIL (UNII: 3W1JG795YI)
  • HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • POLYGLYCERYL-3 OLEATE (UNII: XRQ165498B)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • HEXYL LAURATE (UNII: 4CG9F9W01Q)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Product Labeler Information

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

Labeler Name: Prescriber's Choice Inc.
Labeler Code: 71876
Start Marketing Date: 01-01-2017 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: 12-31-2019 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.

Prescribers Choice Dynamic Broad Spectrum Product Label Images

Prescribers Choice Dynamic Broad Spectrum 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:Prescriber's ChoicePompano Beach, FL 33069

Active Ingredients

Octinoxate 7.5, Zinc Oxide 4.8%

Purpose

Sunscreen

Uses

Help prevent sunburn.

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 use and ask a doctor if rash or irritation 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

Apply liberally and evenly 15 minutes before sun exposure. *Reapply: At least 80 minutes after swimming or sweating, immediately after towel drying, at least every 2 hours. Sun 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 am – 2 pm wear long-sleeve shirts, pants, hats, and sunglasses. *For children under 6 months of age: Ask a doctor.

Inactive Ingredients

Water, Hydrogenated Polybutene, Octyl Stearate, Polyglyceryl-4-Isostearate, Aloe Barbadensis Leaf Extract, Isopropyl Palmitate, Cyclomethicone, Sunflower Oil, Hydrogenated Microcrystalline Wax, Cetyl Dimethicone Copolyol, Cetyl Dimethicone, Hydrogenated Castor Oil, Sodium Chloride, Polyglyceryl-3-Oleate, Silica, Hexyl Laurate, Triethoxycaprylylsilane, Capryly Glycol, Methylisothiazolinone.

Other Information

Store at controlled temperature 15C – 30C (59F-86F). Protect the product in this container from excessive heat and direct sun.

* Please review the disclaimer below.