Femiclear Yeast Infection
Femiclear 2 Day Simple
Organicare Nature's Science, Llc
Human Otc Drug
NDC 71042-026Femiclear Yeast Infection also known as Femiclear 2 Day Simple is a human otc drug labeled by 'Organicare Nature's Science, Llc'. National Drug Code (NDC) number for Femiclear Yeast Infection is 71042-026. This drug is available in dosage form of Ointment. The names of the active, medicinal ingredients in Femiclear Yeast Infection drug includes Cajuput Oil - .1 kg/kg Calendula Officinalis Whole - 1 kg/kg . The currest status of Femiclear Yeast Infection drug is Active.
Drug Information:
| Drug NDC: | 71042-026 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Femiclear Yeast Infection |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Femiclear 2 Day Simple |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Organicare Nature's Science, Llc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Ointment |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | CAJUPUT OIL - .1 kg/kg
CALENDULA OFFICINALIS WHOLE - 1 kg/kg
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
| Marketing Start Date: | 17 Jan, 2023 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 08 May, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Listing Expiration Date: | 31 Dec, 2024 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | OrganiCare Nature's Science, LLC
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | J3TO6BUQ37
PFR03EBU0H
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 71042-026-14 | 1 TUBE in 1 CARTON (71042-026-14) / .0142 kg in 1 TUBE | 17 Jan, 2023 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose healing agent anti-yeast agent anti-microbial and healing agent
Product Elements:
Femiclear yeast infection femiclear 2 day simple calendula officinalis whole calendula officinalis whole pear cajuput oil cajuput oil olive oil yellow wax
Indications and Usage:
Uses treats vaginal yeast infections
Warnings:
Warnings for vaginal use only. femiclear may damage condoms and diaphragms and cause them to fail
Do Not Use:
Warnings for vaginal use only. femiclear may damage condoms and diaphragms and cause them to fail
When Using:
When using this product do not use tampons, douches, spermicides or other vaginal products. condoms and diaphragms may be damaged and fail to prevent pregnancy or sexually transmitted infections (stis) do not have vaginal intercourse mild increase in vaginal burning, itching, or irritation may occur if you do not get complete relief, ask a doctor before using another product
Dosage and Administration:
Directions adults and children 12 years or over: vaginal ointment: use at bed time, read enclosed instructions for complete directions. to protect clothes, use panty liner. fill applicator with vaginal ointment - use one of the tubes lie down in bed. insert applicator into vagina and inject femiclear. remain laying down to avoid leakage. discard applicator after use. do not reuse. repeat on second night - use other tube. children under 12 years: ask a doctor.
Stop Use:
Stop use and ask a doctor if symproms do not get better in 3 days symptoms last more than 7 days you get a rash or hives, abdominal pain, fever, chills, nausea, vomiting or foul-smelling discharge
Package Label Principal Display Panel:
Femiclear yeast infection relieves itching irritation discharge kills >99% of tough to treat yeast* *laboratory testing (non-human/non-animal) homeopathic medicine 2 day dose 2 tubes; net wt 0.25 oz (7.1g) each, total net wt 0.5 oz (14.2g) front panel
Further Questions:
Questions? call 512.401.3572 or vist femiclear.com. organicare, llc, austin tx 78744, usa