NDC 69926-002 Too Cool For School Dino Platz Cinema City (cc Cheek)

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69926-002
Proprietary Name:
Too Cool For School Dino Platz Cinema City (cc Cheek)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
69926
Start Marketing Date: [9]
09-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)

Code Structure Chart

Product Details

What is NDC 69926-002?

The NDC code 69926-002 is assigned by the FDA to the product Too Cool For School Dino Platz Cinema City (cc Cheek) which is product labeled by Too Cool For School Usa, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69926-002-01 1 kit in 1 carton * 30 ml in 1 tube, with applicator * 2.8 g in 1 container. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Too Cool For School Dino Platz Cinema City (cc Cheek)?

Apply liberally 15 minutes before sun exposureUse a water resistant sunscreen if swimming or sweatingReapply at least every 2 hoursSun 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 sunglassesChildren under 6 months : Ask a doctor

Which are Too Cool For School Dino Platz Cinema City (cc Cheek) UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Too Cool For School Dino Platz Cinema City (cc Cheek) Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".