NDC 72588-930 Stubble And Stache Broad Spectrum Spf 30

Octinoxate, Octisalate, Avobenzone

NDC Product Code 72588-930

NDC CODE: 72588-930

Proprietary Name: Stubble And Stache Broad Spectrum Spf 30 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: Octinoxate, Octisalate, Avobenzone 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

  • 72588 - Stubble & Stache Llc.
    • 72588-930 - Stubble And Stache Broad Spectrum Spf 30

NDC 72588-930-03

Package Description: 1 BOTTLE in 1 BOX > 100 mL in 1 BOTTLE

NDC Product Information

Stubble And Stache Broad Spectrum Spf 30 with NDC 72588-930 is a a human over the counter drug product labeled by Stubble & Stache Llc.. The generic name of Stubble And Stache Broad Spectrum Spf 30 is octinoxate, octisalate, avobenzone. The product's dosage form is cream and is administered via topical form.

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.

Stubble And Stache Broad Spectrum 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.


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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • WATER (UNII: 059QF0KO0R)
  • ARGAN OIL (UNII: 4V59G5UW9X)
  • ASCORBYL PALMITATE (UNII: QN83US2B0N)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • CETEARYL OLIVATE (UNII: 58B69Q84JO)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • COCONUT OIL (UNII: Q9L0O73W7L)
  • CUCUMBER (UNII: YY7C30VXJT)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
  • HYALURONIC ACID (UNII: S270N0TRQY)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • SACCHARIDE ISOMERATE (UNII: W8K377W98I)
  • SANTALUM SPICATUM OIL (UNII: H9LVS6REV4)
  • JOJOBA OIL (UNII: 724GKU717M)
  • SORBITAN OLIVATE (UNII: MDL271E3GR)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • CORN (UNII: 0N8672707O)

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: Stubble & Stache Llc.
Labeler Code: 72588
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: 09-14-2018 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: 12-31-2021 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.

Stubble And Stache Broad Spectrum Spf 30 Product Label Images

Stubble And Stache Broad Spectrum 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:

Octinoxate 7.5%, Octisalate 5.0%,


Avobenzone 3.0%

Purpose:

Sunscreen

Indications:

  • 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 skin.

When Using This Product

Keep out of eyes. Rinse with water to remove.

Stop Use And Consult Physician

If irritation or rash develops.

Keep Out Of Reach Of Children.

If product is swallowed, get medical attention or contact poison control center immediately.

Directions:

  • Apply liberally 15-minutes before sun exposure.Reapply:Immediately after swimming, sweating or towel drying.At least every 2 hours.Sun Protection Measure: 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 rating of 15 or higher, along with other sun protection measures including:
  • Limit time in the sun, especially from 10 am to 2 pm.Wear long-sleeved shirts, pants, hats, and sunglasses.For children under 6-months, consult a physician.

Inactive Ingredients:

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Argania Spinosa (Argan) Oil, Ascorbyl Palmitate (Vitamin C), Camellia Sinensis (Green Tea) Extract, Caprylic/Capric Triglyceride, Carbomer, Cetyl Alcohol, Cetearyl Olivate, Citric Acid, Cocos Nucifera (Coconut) Oil, Cucumis Sativus (Cucumber) Extract, Dimethicone, Ethylhexylglycerin, Eucalyptus Globulus Oil, Glycerin, Glyceryl Stearate, Glycyrrhiza Glabra (Licorice) Extract, Helianthus Annuus (Sunflower) Oil, Hyaluronic Acid, Lavandula Angustifolia (Lavender) Oil, Phenoxyethanol, Polysorbate-20, Saccharide Isomerate, Santalum Spicatum (Sandalwood) Oil, Simmondsia Chinensis (Jojoba) Oil, Sorbitan Olivate, Stearyl Alcohol, Tocopheryl Acetate (Vitamin E), Zemea (Corn) Propanediol.

Other Information:

  • Protect this product from excessive heat and direct sun.

* Please review the disclaimer below.