NDC 55910-983 Sunscreen

Avobenzone, Homosalate, Octisalate, Octocrylene

NDC Product Code 55910-983

NDC 55910-983-54

Package Description: 184 g in 1 CAN

NDC Product Information

Sunscreen with NDC 55910-983 is a a human over the counter drug product labeled by Old East Main Co.. The generic name of Sunscreen is avobenzone, homosalate, octisalate, octocrylene. The product's dosage form is spray and is administered via topical form.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Sunscreen 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.

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.

  • ALCOHOL (UNII: 3K9958V90M)

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.

Product Labeler Information

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

Labeler Name: Old East Main Co.
Labeler Code: 55910
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: 01-18-2021 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: 12-31-2023 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 - NO 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.

Sunscreen Product Label Images

Sunscreen 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, Homosalate, Octisalate, Octocrylene




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


For external use only


  • Keep away from fire or flame.after application, wait until product dries before approacing a souce of heat or flame, or before smoking

Do Not Use

  • On damaged or broken skin

Stop Use And Ask A Doctor If

  • Rash occurs

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Conrol Center right away


■ spray liberally and spread evenly by hand 15 minutes before sun exposure■ apply to all skin exposed to the sun■ hold container 4 to 6 inches from the skin to apply■ do not spray directly into face. Spray on hands then apply to face.■ do not apply in windy conditions■ use in a well-ventilated area and avoid inhalation■ reapply:■ after 80 minutes of 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 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 sunglasses■ children under 6 months of age: Ask a doctor

Other Information

  • Protect the product in the container from excessive heat and direct sun

Inactive Ingredients

Alcohol denat., octyldodecyl neopentanoate, acrylates/octylacrylamide copolymer, diethylhexyl 2,6-naphthalate, tocopheryl acetate, fragrance


May stain or damage some fabrics of surfacesDISTRIBUTED BY OLD EAST MAIN CO.100 MISSION RIDGEGOODLETTSVILLE, TN 37072

* Please review the disclaimer below.