NDC 62206-4712 Badger Baby Sunscreen Cream Broad Spectrum Spf 40

Zinc Oxide

NDC Product Code 62206-4712

NDC 62206-4712-8

Package Description: 87 mL in 1 TUBE

NDC Product Information

Badger Baby Sunscreen Cream Broad Spectrum Spf 40 with NDC 62206-4712 is a a human over the counter drug product labeled by W.s. Badger Company, Inc.. The generic name of Badger Baby Sunscreen Cream Broad Spectrum Spf 40 is zinc oxide. 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.

Badger Baby Sunscreen Cream Broad Spectrum Spf 40 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.


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: W.s. Badger Company, Inc.
Labeler Code: 62206
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: 09-24-2021 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.

Badger Baby Sunscreen Cream Broad Spectrum Spf 40 Product Label Images

Badger Baby Sunscreen Cream Broad Spectrum Spf 40 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


Drug Facts

Active Ingredient

Non-Nano Uncoated Zinc Oxide 22.5%




  • 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.


For external use only

Otc - Do Not Use

Do not use on damaged or broken skin. Stop and ask a doctor if rash occurs.

Otc - When Using

When using this product keep out of eyes. Rinse with water to remove.

Otc - Keep Out Of Reach Of Children

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


  • For full protection, apply liberally (2mg/cm
  • 2 of skin) to all exposed skin 15 minutes before sun exposure, then rub in to reduce whitening effect.
  • Reapply: After 40 minutes of swimming or sweatingImmediately after towel dryingAt least every 2 hoursSun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin agingTo 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 10am-2pmWear long-sleeved shirts, pants, hats, and sunglassesFor children under 6 months of age: ask a doctor.


*Helianthus Annuus (
Sunflower) Seed Oil, *Cera Alba (
Beeswax), *Simmondsia Chinensis (
Jojoba) Seed Oil, Tocopherol (
SunflowerVitamin E), *Calendula Officinalis (
Calendula) Flower Extract, *Anthemis Nobilis (
Roman Chammomile) Flower Oil, *Hippophae Rhamnoides (
Seabuckthorn) Fruit Extract.
*= Organic

Other Information

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

* Please review the disclaimer below.