NDC 73231-1901 Summer Ready Innovative Sunscreen

Avobenzone, Homosalate, Octisalate, Octocrylene Cream

NDC Product Code 73231-1901

NDC Code: 73231-1901

Proprietary Name: Summer Ready Innovative Sunscreen 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, Homosalate, Octisalate, Octocrylene Cream 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

  • 73231 - Jada Wellness, Llc
    • 73231-1901 - Summer Ready Innovative Sunscreen

NDC 73231-1901-1

Package Description: 118 mL in 1 TUBE

NDC Product Information

Summer Ready Innovative Sunscreen with NDC 73231-1901 is a a human over the counter drug product labeled by Jada Wellness, Llc. The generic name of Summer Ready Innovative Sunscreen is avobenzone, homosalate, octisalate, octocrylene cream. The product's dosage form is cream and is administered via topical form.

Labeler Name: Jada Wellness, Llc

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Summer Ready Innovative Sunscreen 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 mg/mL
  • HOMOSALATE 6 mg/mL
  • OCTISALATE 4 mg/mL
  • OCTOCRYLENE 7 mg/mL

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.

  • WATER (UNII: 059QF0KO0R)
  • CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
  • ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
  • ETHYLHEXYL PALMITATE (UNII: 2865993309)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • TROLAMINE (UNII: 9O3K93S3TK)

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: Jada Wellness, Llc
Labeler Code: 73231
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: 07-19-2019 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: 12-31-2020 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.

Summer Ready Innovative Sunscreen Product Label Images

Summer Ready Innovative Sunscreen 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

Otc - Active Ingredient

Avobenzone 3%Homosalate 6%Octisalate 4%Octocrylene 7%

Otc - Purpose

Sunscreen

Dosage & Administration

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 sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value 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-sleeved shirts, pants, hats and sunglasses

children under 6 months of age: Ask a doctor

Otc - Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.​

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

Inactive Ingredient

TROLAMINE​ETHYLHEXYL METHOXYCRYLENEETHYLHEXYL PALMITATEETHYLHEXYLGLYCERINPANTHENOLPHENOXYETHANOLSORBITAN SESQUIOLEATESTEARIC ACIDSTEARYL ALCOHOLCARBOMER HOMOPOLYMER, UNSPECIFIED TYPEMEDIUM-CHAIN TRIGLYCERIDESCARBOMER INTERPOLYMER TYPE A (55000 CPS)WATEREDETATE DISODIUM ANHYDROUS​

* Please review the disclaimer below.

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