NDC 76150-293 Sunlight Daily Facial Spf 30

Sunscreen

NDC Product Code 76150-293

NDC 76150-293-34

Package Description: 30 mL in 1 BOTTLE, GLASS

NDC Product Information

Sunlight Daily Facial Spf 30 with NDC 76150-293 is a a human over the counter drug product labeled by Bell International Laboratories, Inc. The generic name of Sunlight Daily Facial Spf 30 is sunscreen. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Bell International Laboratories, Inc

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.

Sunlight Daily Facial Spf 30 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.

  • ZINC OXIDE 12.5 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.

  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
  • GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • ETHYL FERULATE (UNII: 5B8915UELW)
  • CETEARYL OLIVATE (UNII: 58B69Q84JO)
  • COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
  • PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
  • WATER (UNII: 059QF0KO0R)
  • SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
  • LEVOMENOL (UNII: 24WE03BX2T)
  • PHYTATE SODIUM (UNII: 88496G1ERL)
  • HEPTYL UNDECYLENATE (UNII: W77QUB6GXO)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • SQUALANE (UNII: GW89575KF9)
  • SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)
  • COCONUT ALKANES (UNII: 1E5KJY107T)
  • CETYL PALMITATE (UNII: 5ZA2S6B08X)
  • BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
  • GRAPE SEED OIL (UNII: 930MLC8XGG)
  • ETHYLHEXYL OLEATE (UNII: R34927QY59)
  • SHEA BUTTER (UNII: K49155WL9Y)

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: Bell International Laboratories, Inc
Labeler Code: 76150
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: 04-14-2021 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.

Sunlight Daily Facial Spf 30 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

Zinc Oxide 12.5%

Purpose

Sunscreen

Uses

Helps prevent sunburnIf used as directed with other sun 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 skinWhen using this product keep out of eyes. Rinse with water to remove.Stop use and ask a doctor if rash occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Apply liberally 15 minutes before sun exposure. Children under 6 months of age: ask a doctor. Reapply at least every 2 hours. Reapply after swimming or sweating. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrase this risk, regularly use a sunscreen with a Broad Spectrum value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. to 2 p.m.wear long-sleeved shirts, pants, hats, and sunglassesUse a water resistant sunscreen if swimming or sweating.

Other Informaiton

Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients

Bisabolol, Butyloctyl Salicylate, Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Cetearyl Olivate, Cetyl Palmitate, Citric Acid, Coco-Caprylate/Caprate, Coconut Alkanes, Ethyl Ferulate, Ethylhexyl Olivate, Glyceryl Caprylate, Glyceryl Undecylenate, Heptyl Undecylenate, Phenothyl Alcohol. Polyhydroxstearic Acid, Propanediol, Sodium Hyaluronate, Sodium Phytate, Sodium Stearoyl Glutamate, Sorbitan Oleate, Sorbitan Olivate, Sorbitan Palmitate, Squalene, Tocopherol, Triethoxycaprylylsilane, Vitis Vinifera (Grape) Seed Oil, Water, Xanthan Gum

* Please review the disclaimer below.