NDC 82267-010 Arsmedic Step 01 Secret Ampoule

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:
82267-010
Proprietary Name:
Arsmedic Step 01 Secret Ampoule
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Korea Bio Lab Co., Ltd
Labeler Code:
82267
Start Marketing Date: [9]
09-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 82267-010-02

Package Description: 5 VIAL in 1 CARTON / 2 mL in 1 VIAL (82267-010-01)

Product Details

What is NDC 82267-010?

The NDC code 82267-010 is assigned by the FDA to the product Arsmedic Step 01 Secret Ampoule which is product labeled by Korea Bio Lab Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82267-010-02 5 vial in 1 carton / 2 ml in 1 vial (82267-010-01). 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 Arsmedic Step 01 Secret Ampoule?

1. Shake-Take the ampoule from the box and shake gently before use. 2. Never block a hole in the top of the ampoule when opening. Open-Insert the ampoule into the applicator and pressing gently until you hear a 'click'. 3. Remove the applicator device and the top of the ampoule. 4. Position the safety cap up to half the ampoule. 5. Tip half the content on your hands and apply until it is completely absorbed. 6. Cover the ampoule with a small cap if there is a leftover.

Which are Arsmedic Step 01 Secret Ampoule UNII Codes?

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

Which are Arsmedic Step 01 Secret Ampoule 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".