NDC 49358-547 Mdsolarsciences Spf 30 Mineral Tinted

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:
49358-547
Proprietary Name:
Mdsolarsciences Spf 30 Mineral Tinted
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Md Solar Sciences
Labeler Code:
49358
Start Marketing Date: [9]
01-01-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49358-547-01

Package Description: 1 TUBE in 1 CARTON / 48 g in 1 TUBE

Product Details

What is NDC 49358-547?

The NDC code 49358-547 is assigned by the FDA to the product Mdsolarsciences Spf 30 Mineral Tinted which is product labeled by Md Solar Sciences. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49358-547-01 1 tube in 1 carton / 48 g 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 Mdsolarsciences Spf 30 Mineral Tinted?

Shake well. Rub in well.Apply liberally 15 minutes before sun exposureReapply:-After 80 minutes of swimming or sweating-Immeditately after towel drying-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 the risk, regularly use a sunscreen with Broad Spectrum SPF of 15 or higher and other sun protection measures including:-Limit time in the sun, especially from 10a.m. – 2p.m.-Wear long-sleeved shirts, pants, hats and sunglasses

Which are Mdsolarsciences Spf 30 Mineral Tinted UNII Codes?

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

Which are Mdsolarsciences Spf 30 Mineral Tinted 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".