NDC 62802-145 Ocean Potion Quick Dry 30 Sunscreen

Product Information

Product Code62802-145
Proprietary Name 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.
Ocean Potion Quick Dry 30 Sunscreen
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Sun & Skin Care Research, Llc
Labeler Code62802
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
01-01-2012
Listing Expiration Date 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.
12-31-2017
Exclude Flag 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".
I
NDC Code Structure

Usage Information


Product Packages

NDC 62802-145-03

Package Description: 89 mL in 1 BOTTLE

NDC 62802-145-08

Package Description: 237 mL in 1 BOTTLE

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

Product Details

Ocean Potion Quick Dry 30 Sunscreen is product labeled by Sun & Skin Care Research, Llc. The product's dosage form is and is administered via form.


What are Ocean Potion Quick Dry 30 Sunscreen Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • HOMOSALATE (UNII: V06SV4M95S)
  • HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
  • OCTISALATE (UNII: 4X49Y0596W)
  • OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
  • OCTOCRYLENE (UNII: 5A68WGF6WM)
  • OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
  • AVOBENZONE (UNII: G63QQF2NOX)
  • AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)


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)
  • CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
  • CHOLECALCIFEROL (UNII: 1C6V77QF41)
  • DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
  • DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • HYPROMELLOSE 2208 (15000 MPA.S) (UNII: Z78RG6M2N2)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
  • ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • TROLAMINE (UNII: 9O3K93S3TK)


* Please review the disclaimer below.

Ocean Potion Quick Dry 30 Sunscreen Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Active Ingredients




Homosalate: 12%
Octisalate: 5%
Octocrylene: 5%
Avobenzone: 3%



Purpose



Sunscreen


Uses



  • helps prevent sunburn
  • If used as directed with other skin protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings



For external use only.  Do not use on damaged or broken skin. Stop use and ask a doctor if rash occurs. When using this product keep out of eyes.  Rinse with water to remove. Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


Directions



  • apply liberally 15 minutes before sun exposure
  • reapply after 80 minutes of swimming or sweating and 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 value of 15 or higher and other sun protection measures including limiting time in the sun, especially from 10a.m.-2p.m., wear long-sleeved shirts, pants hats and sunglasses.
  • children under 6 months: Ask a doctor

Other Information



  • For use on skin only
  • Avoid contact with fabric
  • Protect this product from excessive heat and direct sun

Package Label.Principal Display Panel







* Please review the disclaimer below.