NDC 49035-859 Eqaute Beauty Ultra Light Sunscreen Spf 70

Avobenzone, Homosalate,octisalate,octocrylene,oxybenzone

NDC Product Code 49035-859

NDC Code: 49035-859

Proprietary Name: Eqaute Beauty Ultra Light Sunscreen Spf 70 Additional informationCallout TooltipWhat 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, Homosalate,octisalate,octocrylene,oxybenzone Additional informationCallout TooltipWhat 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.


Code Structure
  • 49035 - Walmart Stores Inc.
    • 49035-859 - Eqaute Beauty Ultra Light Sunscreen Spf 70

NDC 49035-859-36

Package Description: 42 g in 1 TUBE

NDC Product Information

Eqaute Beauty Ultra Light Sunscreen Spf 70 with NDC 49035-859 is a a human over the counter drug product labeled by Walmart Stores Inc.. The generic name of Eqaute Beauty Ultra Light Sunscreen Spf 70 is avobenzone, homosalate,octisalate,octocrylene,oxybenzone. The product's dosage form is stick and is administered via topical form.

Labeler Name: Walmart Stores Inc.

Dosage Form: Stick - A dosage form prepared in a relatively long and slender often cylindrical form.

Product Type: Human Otc Drug Additional informationCallout TooltipWhat 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.


Eqaute Beauty Ultra Light Sunscreen Spf 70 Active Ingredient(s)

Additional informationCallout TooltipWhat 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 30 mg/g
  • HOMOSALATE 150 mg/g
  • OCTISALATE 50 mg/g
  • OCTOCRYLENE 100 mg/g
  • OXYBENZONE 30 mg/g

Inactive Ingredient(s)

Additional informationCallout TooltipAbout 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.

  • ADIPIC ACID/DIGLYCOL CROSSPOLYMER (20000 MPA.S) (UNII: R9TPS68K19)
  • BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
  • NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW)
  • OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
  • PARAFFIN (UNII: I9O0E3H2ZE)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Administration Route(s)

Additional informationCallout TooltipWhat 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

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Walmart Stores Inc.
Labeler Code: 49035
FDA Application Number: part352 Additional informationCallout TooltipWhat 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. Additional informationCallout TooltipWhat 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: 02-13-2019 Additional informationCallout TooltipWhat 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: 12-31-2020 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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.

Eqaute Beauty Ultra Light Sunscreen Spf 70 Product Label Images

Eqaute Beauty Ultra Light Sunscreen Spf 70 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%,Homosalate 15%,Octisalate 5%,Octocrylene 10%,Oxybenzone 3%

Purpose

Sunscreen

Warnings

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 Center right away.

Directions

• apply liberally 15 minutes before sun exposure• reapply:• after 80 minutes of swimming or sweating• immediately after towel drying• at least every 2 hours• children under 6 months of age: ask a doctor• 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 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-sleeve shirts, pants, hats, and sunglasses

Other Information

• protect this product from excessive heat and direct sun• may stain or damage some fabrics, materials or surfaces

Inactive Ingredients

Adipic adic/diglycol crosspolymer, beeswax, butyloctyl salicylate, C12-15 alkyl benzoate, caprylyl glycol, dimethicone, fragrance, neopentylglycol diethylhexanoate, neopentyl glycol diisostearate, octydodecyl neopentanoate, ozokerite, paraffin, polyethylene, silica

Other

Equate Beauty Ultra Light Sunscreen Stick Broad Spectrum SPF 70 provides water resistant UVA/UVB protection specifically formulated for beach fun! This no mess, hands-free stick contains a lightweight formula that glides on easily and absorbs quickly - leaving skin moisturized, protected,and refreshed

Prinicipal Dispaly Panel

Eqaute Beauty Compare to NEUTROGENA ® ULTRA SHEER® SUNSCREEN STICKUltra LightSunscreenSTICK SPF 70Broad Spectrum SPF 70 protection Water resistant (80 minutes) • Dermatologist testedPARABEN FREENET WT 1.5 OZ (42 g)

* Please review the disclaimer below.

Previous Code
49035-858
Next Code
49035-860