NDC 47124-450 Sunscreen Spf 30 Wegmans

Avobenzone - 3.0% Homosalate - 10.0% Octisalate - 5.0% Octocrylene - 10.0%

NDC Product Code 47124-450

NDC 47124-450-05

Package Description: 117 mL in 1 BOTTLE

NDC Product Information

Sunscreen Spf 30 Wegmans with NDC 47124-450 is a a human over the counter drug product labeled by Wegman. The generic name of Sunscreen Spf 30 Wegmans is avobenzone - 3.0% homosalate - 10.0% octisalate - 5.0% octocrylene - 10.0%. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Wegman

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.

Sunscreen Spf 30 Wegmans 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 3 g/100mL
  • HOMOSALATE 10 g/100mL
  • OCTISALATE 5 g/100mL
  • OCTOCRYLENE 10 g/100mL

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.

  • OLETH-3 (UNII: BQZ26235UC)
  • SORBITOL (UNII: 506T60A25R)
  • WATER (UNII: 059QF0KO0R)
  • POLYAMIDE-8 (4500 MW) (UNII: 77723GV81A)

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: Wegman
Labeler Code: 47124
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 NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 01-03-2013 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: 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.

Sunscreen Spf 30 Wegmans Product Label Images

Sunscreen Spf 30 Wegmans 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                         Purpose

Avobenzone 3%...........................SunscreenHomosalate 10%..........................SunscreenOctisalate 5%.......................... ....SunscreenOctocrylene 10%..........................Sunscreen


For external use onlyDo not use on damaged or broken skinWhen using this product keep out of eyes. Rinse with water to remove.Stop use and ask a doctor if rash occursKeep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.


• apply liberally 15 minutes before sun exposure• reapply: • after 80 minutes of swimming or sweating• immediately after towel drying • at least every 2 hours• Sun Protection Measures. Spending time in the sunincreases your risk of skin cancer and early skin aging.To decrease this risk, regularly use a sunscreen with abroad spectrum SPF of 15 or higher and other sunprotection measures including:• limit time in the sun, especially from 10 a.m. – 2 p.m.• wear long-sleeve shirts, pants, hats, and sunglasses• children under 6 months: Ask a doctor

Inactive Ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzyl Alcohol, Caprylic/Capric Triglyceride, Chlorphenesin, Diethylhexyl Syringylidenemalonate, Disodium EDTA, Ethylhexyl Palmitate, Fragrance, Oleth-3, Polyamide-8, Sodium Ascorbyl Phosphate, Sorbitol, Tocopherol, Triethanolamine, Water.

Other Information

• protect this product from excessive heat and direct sun • may stain fabrics.Questions or comments?1-800-Wegmans(934-6267) Ext 59209am - 4pm EST weekdays.

* Please review the disclaimer below.