NDC 58633-233 Cc Spf 18 Medium

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:
58633-233
Proprietary Name:
Cc Spf 18 Medium
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dr. Dennis Gross Skincare, Llc
Labeler Code:
58633
Start Marketing Date: [9]
07-15-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)

Product Packages

NDC Code 58633-233-10

Package Description: 1 TUBE in 1 CARTON / 30 mL in 1 TUBE

NDC Code 58633-233-60

Package Description: 7 mL in 1 TUBE

Product Details

What is NDC 58633-233?

The NDC code 58633-233 is assigned by the FDA to the product Cc Spf 18 Medium which is product labeled by Dr. Dennis Gross Skincare, Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 58633-233-10 1 tube in 1 carton / 30 ml in 1 tube, 58633-233-60 7 ml in 1 tube . 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 Cc Spf 18 Medium?

Apply liberally 15 minutes before sun exposureuse a water resistant sunscreen if swimming or sweatingreapply at least every 2 hourschildren under 6 months: Ask a doctorSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use of 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

Which are Cc Spf 18 Medium UNII Codes?

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

Which are Cc Spf 18 Medium 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:

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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".