NDC 73440-2154 Sea And Ski Spf 50

Avobenzone, Homosalate, Octisalate, Octocrylene

NDC Product Code 73440-2154

NDC 73440-2154-1

Package Description: 42.5 g in 1 TUBE

NDC Product Information

Sea And Ski Spf 50 with NDC 73440-2154 is a a human over the counter drug product labeled by Cross Brands Contract Filling. The generic name of Sea And Ski Spf 50 is avobenzone, homosalate, octisalate, octocrylene. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Cross Brands Contract Filling

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Sea And Ski Spf 50 Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • AVOBENZONE 1.275 g/42.5g
  • OCTISALATE 2.975 g/42.5g
  • HOMOSALATE 6.375 g/42.5g
  • OCTOCRYLENE 3.4 g/42.5g

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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Cross Brands Contract Filling
Labeler Code: 73440
FDA Application Number: part352 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-25-2020 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: 12-31-2021 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: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Sea And Ski Spf 50 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

Active Ingredients

Avobenzone 3.0%, Homsalate 15.0%, Octisalate 7.0%, Octocrylene 8.0%




Helps prevent sunburn. if used as directed with other sun protection measures (see
Directions), decreases the reisk of skin cancer and early skin aging caused by the sun


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 occurs

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Cener right away.


  • Apply liberally 15 minutes before sun exposure. reapply:after 80 minutes of swimming or swetingimmediately after towl 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 value 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-sleeved shirts, pants, hats and sunglassesChildren under 6 months: Ask a doctor.

Other Information

Protect this product from excessive heat and direct sunmay stain some fabrics, wood, plastics, vinylfor use on skin onlystore between 20°-25°C (68°-77°F).


Acrylates copolymer, acrylates/c10-30 alkyl acrylate crosspolymer, aloe barbadensis leaf juice, butylene glycol, carbomer, dimethicone, disodium EDTA, ethylhexyl palmitate, ethylhexylglycerin, glycerin, hydroxypropyl methylcellulose, neopentyl glycol diheptanoate, phenoxyethanol, simmondsia chinensis (jojoba) extract, sorbitan monooleate, styrene/ acrylates copolymer, triethanolamine, water

* Please review the disclaimer below.