NDC 54860-383 Quiksilver Spf 30 Sunscreen 01

Avobenzone, Ethylhexyl Methoxycinnamate, Homosalate, Octocrylene

NDC Product Code 54860-383

NDC CODE: 54860-383

Proprietary Name: Quiksilver Spf 30 Sunscreen 01 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.

Non-Proprietary Name: Avobenzone, Ethylhexyl Methoxycinnamate, Homosalate, Octocrylene What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 54860 - Shenzhen Lantern Scicence Co.,ltd.

NDC 54860-383-01

Package Description: 30 g in 1 BOTTLE, PLASTIC

NDC Product Information

Quiksilver Spf 30 Sunscreen 01 with NDC 54860-383 is a a human over the counter drug product labeled by Shenzhen Lantern Scicence Co.,ltd.. The generic name of Quiksilver Spf 30 Sunscreen 01 is avobenzone, ethylhexyl methoxycinnamate, homosalate, octocrylene. The product's dosage form is lotion and is administered via topical form.

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.

Quiksilver Spf 30 Sunscreen 01 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.

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: Shenzhen Lantern Scicence Co.,ltd.
Labeler Code: 54860
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: 09-14-2021 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: 12-31-2022 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.

Quiksilver Spf 30 Sunscreen 01 Product Label Images

Quiksilver Spf 30 Sunscreen 01 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 Ingredient

Active Ingredient PurposeAvobenzone 1.0%Ethylhexyl Methoxycinnamate 8.0%Homosalate 2.0%Octocrylene 2.0% ..........................................Sunscreen

Inactive Ingredients



Apply liberaaly 15 minutes before sun exposure.Children under 6 months; Ask a doctor.

Otc - Do Not Use

When using this productkeep out of eyes. In case of contact with eyes, flush thoroughly with water.Do not inhale or ingest.Avoid contact with broken skin.

Other Information

Do not store above 105F.May discolor some fabrics. Harmful to wood finishes and plastics.

Protect the product in this container from excessive heat and direct sun.For sunscreen useApply to all skin exposed to the sunLimit time in the sun,especially from 10 a.m.-2 p.m.Wear long-s;eeved shirts,pants,hats,and sunglasses.

When Using This Product

Keep out of eyes,Rinse with water to remove.



Stop Use And Ask A Doctor

If rash occurs.

Do Not Use

On danaged or broken skin.

* Please review the disclaimer below.