NDC 71042-031 Femiclear Yeast Infection 2 Day Dose

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:
71042-031
Proprietary Name:
Femiclear Yeast Infection 2 Day Dose
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
71042
Start Marketing Date: [9]
04-28-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 71042-031?

The NDC code 71042-031 is assigned by the FDA to the product Femiclear Yeast Infection 2 Day Dose which is product labeled by Organicare Nature's Science, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71042-031-28 1 kit in 1 carton * 14 g in 1 tube (71042-034-14) * 14 g in 1 tube (71042-035-14). 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 Femiclear Yeast Infection 2 Day Dose?

Usestreats vaginal yeast infectionsrelieves external itching and irritation due to a vaginal yeast infection

Which are Femiclear Yeast Infection 2 Day Dose UNII Codes?

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

  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
  • OLEUROPEIN (UNII: 2O4553545L)
  • OLEUROPEIN (UNII: 2O4553545L) (Active Moiety)
  • MELALEUCA CAJUPUTI LEAF OIL (UNII: 5O59RMR6DU)
  • MELALEUCA CAJUPUTI LEAF OIL (UNII: 5O59RMR6DU) (Active Moiety)
  • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
  • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)

Which are Femiclear Yeast Infection 2 Day Dose 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".