NDC 73113-050 Pedatosol Oattbe Syn Bio Beta Glucans Derma Blemish Balm

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:
73113-050
Proprietary Name:
Pedatosol Oattbe Syn Bio Beta Glucans Derma Blemish Balm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
73113
Start Marketing Date: [9]
12-01-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 73113-050?

The NDC code 73113-050 is assigned by the FDA to the product Pedatosol Oattbe Syn Bio Beta Glucans Derma Blemish Balm which is product labeled by Mh Global Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73113-050-02 1 container in 1 carton / 50 ml in 1 container (73113-050-01). 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 Pedatosol Oattbe Syn Bio Beta Glucans Derma Blemish Balm?

BB Cream protects skin with SPF 15 so you can wear a moisturizer and sunscreen in one convenient beauty product. ■ Apply on all exposed areas 15-20 minutes before sun exposure. ■ Re-apply often (every 2 hours) and after swimming, excessive perspiration and washing to ensure maximum sun protection.

Which are Pedatosol Oattbe Syn Bio Beta Glucans Derma Blemish Balm UNII Codes?

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

Which are Pedatosol Oattbe Syn Bio Beta Glucans Derma Blemish Balm 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".