Home › NDC Lookup › Ingredients › Kreosotum 6C, Nitricum Acidum 6C, Thuja... › 73716-0001-10
BiopHresh Kreosotum 6C, Nitricum Acidum 6C, Thuja Occidentalis 6C, Pulsatilla Vulgaris 6C, Sepia Officinalis 6C 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g Suppository, 1 g — NDC 73716-0001-10 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

BiopHresh Kreosotum 6C, Nitricum Acidum 6C, Thuja Occidentalis 6C, Pulsatilla Vulgaris 6C, Sepia Officinalis 6C 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g Suppository, 1 g — NDC 73716-001-10 (Billing 73716-0001-10)

by Good Clean Love, Inc. · 1 g in 1 BLISTER PACK

This is a package of 1 g of BiopHresh Kreosotum 6C, Nitricum Acidum 6C, Thuja Occidentalis 6C, Pulsatilla Vulgaris 6C, Sepia Officinalis 6C 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g Suppository from Good Clean Love, Inc., marketed since Apr 2020 and currently FDA-listed. It is this product's only package size.

NDC 73716-0001-10
🏷️ FDA NDC (as labeled) 73716-001-10 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 73716-001-10 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
73716 labeler · 001 product · 10 package
Package marketed since
Apr 17, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7371600110 5
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 73716-001-10
Product NDC 73716-001
11-digit billing NDC 73716000110
UNII 1NT28V9397, I76KB35JEV, 48GD5780QF, 3JYG22FD73, 411VRN1TV4
SPL Set ID a3ae582a-edb1-3a46-e053-2995a90a901a
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-04-17
Route VAGINAL
Dosage form SUPPOSITORY
Substance THUJA OCCIDENTALIS LEAFY TWIG; PULSATILLA VULGARIS; SEPIA OFFICINALIS WHOLE; WOOD CREOSOTE; NITRIC ACID
Why two NDCs? The FDA registers this code as 73716-001-10 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 73716-0001-10. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

BiopHresh Kreosotum is a homeopathic suppository formulated for vaginal use containing five plant and mineral-derived ingredients in homeopathic dilution. The product includes wood creosote, nitric acid, pulsatilla, sepia, and thuja, which are used in homeopathic practice for various purposes. This is an unapproved homeopathic product marketed based on homeopathic tradition rather than FDA evaluation for effectiveness.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
73716-0001-10 You're viewing this Main listing 1 g in 1 BLISTER PACK 2020-04-17 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
BiopHresh 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/gthis 73716-0001-10 Good 1 g — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2020
On the market since
Apr 2020
📍
2026
Currently FDA-listed
6 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII PQ6CK8PD0R
    Ascorbic acid, also known as vitamin C, is a white crystalline powder. It serves as an antioxidant to prevent degradation of other ingredients and may also function as a preservative in the formulation.
  • UNII 2G86QN327L
    Gelatin is a protein derived from animal collagen, commonly used in medicines as a gelling agent and capsule material. It helps create soft or hard capsule shells that hold and release medication, and can also thicken liquid formulations.
  • UNII 1PRR1V42V5
    A beneficial bacterium sometimes added to medicines and supplements. It may serve as a probiotic ingredient intended to support digestive health, though in a medicine it functions mainly as an active component rather than a traditional inactive filler or binder.
  • UNII QX2H2M2084
    A beneficial bacterium used as a probiotic ingredient. It helps maintain the product's stability and may support the formulation's intended microbial balance when delivered to the body.
  • UNII Q66E0D2443
    A live microorganism strain used as a probiotic ingredient. It's included to support beneficial bacteria in the digestive system and improve product stability.
  • UNII QFC21096ON
    A beneficial bacteria strain used as a probiotic active or functional ingredient. It may help support gut health and digestion, though in this formulation it serves as a live microbial component rather than a traditional inactive filler or binder.
  • UNII 9913I24QEE
    A live beneficial bacterium added to some medicines and supplements. It serves as a probiotic ingredient intended to support gut health and digestion.
  • UNII 9601IVB87J
    A beneficial bacterium commonly used in probiotic supplements. It serves as an active microorganism that supports the product's intended probiotic function by promoting healthy gut bacteria balance.
  • UNII 7A4S6N2EG2
    A beneficial bacterium added to support the product's probiotic content. It serves as an active microbial ingredient intended to promote digestive or oral health when the medicine is taken as directed.
  • UNII 7CVR7L4A2D
    A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
  • UNII 24SC3U704I
    A powdery carbohydrate extracted from tapioca plant roots. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your digestive system.

11 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesInactive ingredients Ascorbic Acid, Gelatin, Lactobacillus acidophilus LA02, Lactobacillus crispatus LCR01, Lactobacillus gasseri LGS06, Limosilactobacillus fermentum LF08, Lactiplantibacillus plantarum LP01, Lacticaseibacillus rhamnosus LR06, Ligilactobacillus salivarius CRL1328, Maltodextrin, Tapioca starch

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerGood Clean Love, Inc.
Labeler code73716
First marketedApr 2020
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from Good Clean Love, Inc. labeler code 73716

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 39 words ▾

Uses for the temporary relief of symptoms of bacterial vaginosis due to bacterial imbalance in the vagina including unusual vaginal odor, itching, irritaiton, or abnormal discharge. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

⏱️ Dosage and Administration 67 words ▾

Directions Wash hands before use When the vaginal area is clean and dry, use either your finger or providede applicator to insert capsule as far as is comfortable Adults 18 years of age and over: insert one suppository into the vagina every 3 days as needed before bedtime to relieve symptoms of bacterial vaginosis and to support vaginal flora. Under 18 years of age: consult a doctor

⚠️ Warnings 143 words ▾

For Vaginal Use Only Do not use with other vaginal suppositories during menstruation or with use of a tampon Ask a doctor before use if you have vaginal itching and discomfort for the first time lower abdominal, back or shoulder pain, fever, chills, nausea, vomiting, or foul smelling vaginal discharge. You may have a more serious condition. been exposed to the human immunodeficiency virus (HIV) that causes AIDS or any other sexually transmitted disease. Stop use and ask doctor if symptoms do not get better in 7 days symptoms last more than 14 days you ge a rash or hives, abdominal pain, fever, chills, nausea, vomiting, or foul smelling vaginal discharge If pregnant, trying to conceive, or breastfeeding consult your doctor before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

📦 Storage and Handling 23 words ▾

Storage instructions ​Does not require refrigeration, and best to store in a cool, dry place at a temperature of 15-30 C (50-86 F).

🧪 Active Ingredient 34 words ▾

Kreosotum 6C HPUS* Nitricum Acidum 6C HPUS* Thuja Occidentalis 6C HPUS* Pulsatilla Pratensis 6C HPUS* Sepia Officinalis 6C HPUS* *"HPUS" indicates the active ingredients are in the official Homeopathic Pharmacopeia of the United States.

🧪 Inactive Ingredients 29 words ▾

Inactive ingredients Ascorbic Acid, Gelatin, Lactobacillus acidophilus LA02, Lactobacillus crispatus LCR01, Lactobacillus gasseri LGS06, Limosilactobacillus fermentum LF08, Lactiplantibacillus plantarum LP01, Lacticaseibacillus rhamnosus LR06, Ligilactobacillus salivarius CRL1328, Maltodextrin, Tapioca starch

🎯 Purpose 39 words ▾

Kreosotum 6C HPUS* Nitricum Acidum 6C HPUS*................Vaginal Itching and Irritation Thuja Occidentalis 6C HPUS* Pulsatilla Pratensis 6C HPUS*................Vaginal Odor Sepia Officinalis 6C HPUS*................Vaginal Discharge *"HPUS" indicates the active ingredients are in the official Homeopathic Pharmacopeia of the United States.

📄 Do Not Use 15 words ▾

Do not use with other vaginal suppositories during menstruation or with use of a tampon

📄 Ask a Doctor Before Use If 55 words ▾

Ask a doctor before use if you have vaginal itching and discomfort for the first time lower abdominal, back or shoulder pain, fever, chills, nausea, vomiting, or foul smelling vaginal discharge. You may have a more serious condition. been exposed to the human immunodeficiency virus (HIV) that causes AIDS or any other sexually transmitted disease.

📄 Stop Use and Ask a Doctor If 37 words ▾

Stop use and ask doctor if symptoms do not get better in 7 days symptoms last more than 14 days you ge a rash or hives, abdominal pain, fever, chills, nausea, vomiting, or foul smelling vaginal discharge

🤰 If Pregnant or Breast-Feeding 12 words ▾

If pregnant, trying to conceive, or breastfeeding consult your doctor before use.

📄 Keep Out of Reach of Children 20 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

📄 Other Information 21 words ▾

Other information tamper resistant for your protection. Use only if safety seal is intact. do not purchase if carton is open

📄 Questions or Comments 30 words ▾

Questions or comments? 1-541-344-4483 Monday through Friday, 9 a.m. - 5 p.m. PST or visit our website at www.goodcleanlove.com. You may also report serious side effects to this phone number.

📄 Package Label / Principal Display Panel 25 words ▾

Good Clean Love biopHresh vaginal homeopathic suppositor Helps Relieve Symptoms of Bacterial Vaginosis BIO-MATCH TECHNOLOGY WORKS THE WAY YOU DO. 10 Gelatin Suppositories 1 2

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

BiopHresh Kreosotum 6C, Nitricum Acidum 6C, Thuja Occidentalis 6C, Pulsatilla Vulgaris 6C, Sepia Officinalis 6C 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g; 6 [hp_C]/g SUPPOSITORY is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Homeopathic". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Good Clean Love, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Good Clean Love, Inc. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 73715-0007-01 · Mohnark 73716-0003-05 · Good →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.