NDC 71609-0003 Moistie Cell Plus

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:
71609-0003
Proprietary Name:
Moistie Cell Plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
71609
Start Marketing Date: [9]
09-30-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 71609-0003?

The NDC code 71609-0003 is assigned by the FDA to the product Moistie Cell Plus which is product labeled by Purecell Korea Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71609-0003-1 10 ml in 1 syringe, plastic . 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 Moistie Cell Plus?

1. After cleansing, massage slowly along your face skin's texture. (After cleansing, You can do it after applying your skin softner) 2. Forehead Massage with proper pressure of the finger from top to bottom in one direction. 3. Chin Massage with proper pressure of the fingers from top to bottom, or from side to side in one direction. 4. Cheek Massage the finger at the proper pressure only in one direction from the lower jaw to the upper jaw along the skin's texture. 5. Finish, with lotion or cream after fever disappears. you can make up. It is usually done in the evening or at night. 6. After the heat is gone, finish with lotion or cream. It is usually done in the evening or at night. (You can use it once a week even if it is used in dermatology)

Which are Moistie Cell Plus UNII Codes?

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

Which are Moistie Cell Plus 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".