NDC 49035-629 Equate Beauty Ultra Light Sunscreen Spf70 Broad Spectrum

Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone

NDC Product Code 49035-629

NDC Code: 49035-629

Proprietary Name: Equate Beauty Ultra Light Sunscreen Spf70 Broad Spectrum 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
    • 49035-629 - Equate Beauty Ultra Light Sunscreen Spf70

NDC 49035-629-09

Package Description: 89 mL in 1 TUBE

NDC Product Information

Equate Beauty Ultra Light Sunscreen Spf70 Broad Spectrum with NDC 49035-629 is a a human over the counter drug product labeled by Walmart. The generic name of Equate Beauty Ultra Light Sunscreen Spf70 Broad Spectrum is avobenzone, homosalate, octisalate, octocrylene, oxybenzone. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Walmart

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 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.


Equate Beauty Ultra Light Sunscreen Spf70 Broad Spectrum 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 3 g/89mL
  • HOMOSALATE 10 g/89mL
  • OCTISALATE 3 g/89mL
  • OCTOCRYLENE 7 g/89mL
  • OXYBENZONE 6 g/89mL

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.

  • WATER (UNII: 059QF0KO0R)
  • ACRYLIC ACID (UNII: J94PBK7X8S)
  • POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • CAPRYLYL TRIMETHICONE (UNII: H6HK6E4EB1)
  • POLYSILICONE-15 (UNII: F8DRP5BB29)
  • CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
  • GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
  • TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
  • SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
  • ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
  • TRIDECETH-6 (UNII: 3T5PCR2H0C)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)

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
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: 01-17-2019 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.

Equate Beauty Ultra Light Sunscreen Spf70 Broad Spectrum Product Label Images

Equate Beauty Ultra Light Sunscreen Spf70 Broad Spectrum 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

AVOBENZONE 3.0%HOMOSALATE 10.0%OCTISALATE 3.0%OCTOCRYLENE 7.0%OXYBENZONE 6.0%

Inactive Ingredients

Water, styrene/acrylates copolymer, dimethicone, acrylates/C12-22 alkyl methacrylate copolymer, propylene glycol, xantham gum, caprylyl methicone, polysilicone-15, cetyl dimethicone, glyceryl stearate, PEG-100 stearate, beeswax, silica, dipotassium glycyrrhizate, trimethylsiloxysilicate, sodium polyacrylate, ethylhexyl stearate, trideceth-6,phenoxyethanol, caprylyl glycol, ethylhexylglycerin, disodium EDTA,  and fragrance

Purpose

AVOBENZONE 3.0%     SunscreenHOMOSALATE 10.0%   SunscreenOCTISALATE 3.0%      SunscreenOCTOCRYLENE 7.0%    SunscreenOXYBENZONE 6.0%    Sunscreen

Uses

  • Helps prevent sunburnif used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and and early aging caused by the sun

Warnings

For external use only.Do not use  - 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.

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

* Please review the disclaimer below.

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