Home › NDC Lookup › Ingredients › Aesculus Hippocastanum, Flos, Ferrum Pho... › 69779-0012-02
sleep Aesculus hippocastanum, flos, Ferrum Phos, Kali Carb, Kali Phos, Mag Phos, Nat Mur, Populus termula, flos, Prunus cerasifera, flos 5 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_C]/29.6mL; 6 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_X]/ Spray, 1 bottle — NDC 69779-0012-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

sleep Aesculus hippocastanum, flos, Ferrum Phos, Kali Carb, Kali Phos, Mag Phos, Nat Mur, Populus termula, flos, Prunus cerasifera, flos 5 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_C]/29.6mL; 6 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_X]/ Spray, 1 bottle — NDC 69779-012-02 (Billing 69779-0012-02)

by Siddha Flower Essences LLC · 1 BOTTLE in 1 CARTON / 7.5 mL in 1 BOTTLE

This is a package of 1 bottle of sleep Aesculus hippocastanum, flos, Ferrum Phos, Kali Carb, Kali Phos, Mag Phos, Nat Mur, Populus termula, flos, Prunus cerasifera, flos 5 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_C]/29.6mL; 6 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_X]/ Spray from Siddha Flower Essences LLC, marketed since Apr 2015 and currently FDA-listed.

NDC 69779-0012-02
🏷️ FDA NDC (as labeled) 69779-012-02 billing pads the product segment with a zero
This package
Contains1 bottle Pack sizes2 compare ↓
Product page 69779-0012-01 Also comes in: 29.6 mL 69779-012-01
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 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 69779-012-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69779 labeler · 012 product · 02 package
Package marketed since
Apr 3, 2019
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0897186002016
FDA record last changed
Oct 1, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69779-012-02
Product NDC 69779-012
11-digit billing NDC 69779001202
UNII KK0Z92II8M, 91GQH8I5F7, BQN1B9B9HA, CI71S98N1Z, HF539G9L3Q, 451W47IQ8X +2 more
UPC 0897186002016
SPL Set ID dc353895-3a58-475c-8afd-ab08b27b96c3
Established class (EPC) Calculi Dissolution Agent; Inhibition Large Intestine Fluid/E
Physiologic effect Increased Large Intestinal Motility; Inhibition Large Intestine Fluid/Electrolyte Absorption
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-04-09
Route ORAL
Dosage form SPRAY
Substance AESCULUS HIPPOCASTANUM FLOWER; FERROSOFERRIC PHOSPHATE; POTASSIUM CARBONATE; POTASSIUM PHOSPHATE, DIBASIC; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SODIUM CHLORIDE; POPULUS TREMULA FLOWERING TOP; PRUNUS CERASIFERA FLOWER
Why two NDCs? The FDA registers this code as 69779-012-02 — 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 → 69779-0012-02. 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?

This is an oral spray product marketed as a homeopathic preparation based on homeopathic tradition rather than FDA evaluation for effectiveness. It contains multiple ingredients including flower extracts from horse chestnut, poplar, and cherry plum, along with mineral salts like ferrous phosphate, magnesium phosphate, potassium salts, and sodium chloride. In homeopathic practice, these ingredients are traditionally used to support sleep and relaxation, though homeopathic products are not evaluated by the FDA to confirm these uses work as claimed. Homeopathic products rely on traditional use rather than clinical evidence of safety or 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 mLPer 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.
Try another pack size: 29.6 mL
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
69779-0012-01 69779-012-01 Main listing 1 BOTTLE in 1 CARTON / 29.6 mL in 1 BOTTLE 2015-04-09 — Active
69779-0012-02 You're viewing this 1 BOTTLE in 1 CARTON / 7.5 mL in 1 BOTTLE 2019-04-03 — Active

Pack size FAQ

What quantity is in this package?
This package contains 1 bottle — 1 bottle in 1 carton / 7.5 ml in 1 bottle.
How does this package differ from NDC 69779-0012-01?
Both are sleep Aesculus hippocastanum, flos, Ferrum Phos, Kali Carb, Kali Phos, Mag Phos, Nat Mur, Populus termula, flos, Prunus cerasifera, flos 5 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_C]/29.6mL; 6 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_X]/ Spray — the drug itself is identical. This page's package is the 1 bottle one, while NDC 69779-0012-01 is the 1 bottle package.
What NDC number is used to bill for this package of sleep Aesculus hippocastanum, flos, Ferrum Phos, Kali Carb, Kali Phos, Mag Phos, Nat Mur, Populus termula, flos, Prunus cerasifera, flos 5 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_C]/29.6mL; 6 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_X]/ Spray?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
sleep 5 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_C]/29.6mL; 6 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_X]/this 69779-0012-02 Siddha 1 bottle — — 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

🏛️
2015
On the market since
Apr 2015
📍
2026
Currently FDA-listed
11 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerSiddha Flower Essences LLC
Labeler code69779
First marketedApr 2015
Product typeHuman Otc Drug
Portfolio21 products on file

More NDCs from Siddha Flower Essences LLC labeler code 69779

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 📋 Description 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 31 words ▾

Uses temporarily relieves symptoms of occasional sleeplessness agitated sleep sleeplessness from mental exertion drowsiness during day anxious dreams persistent unwanted thoughts indications are based on homeopathic materia medica, not clinical tests.

⏱️ Dosage and Administration 71 words ▾

Directions spray in mouth at bedtime for maximum effect spray in mouth one hour before bed and again at bedtime can also be used after waking up in the middle of the night use 5 days per week until symptoms are relieved adults and children 12 years and over 4-5 sprays per dose children 2 years to under 12 years 2-3 sprays per dose children under 2 years consult a doctor

⚠️ Warnings 28 words ▾

Warnings Stop use and ask a doctor if symptoms persist or worsen If pregnant or breast-feeding ask a health professional before use Keep out of reach of children

📦 Storage and Handling 20 words ▾

Other Information do not use if plastic seal around cap is broken or missing. store in a cool, dry place.

🧪 Active Ingredient 46 words ▾

Active Ingredient Each dose contains equal parts of: Aesculus hippocastanum, flos (White Chestnut) 5X HPUS Ferrum Phos 12X HPUS Kali Carb 6C HPUS Kali Phos 6X HPUS Mag Phos 12X HPUS Nat Mur 6X HPUS Populus termula, flos (Aspen) 5X HPUS Prunus cerasifera, flos 5X HPUS

🧪 Inactive Ingredients 17 words ▾

Inactive Ingredients Dandelion*, German Chamomile*, Licorice*, Lotus*, Natural Flavor, Purified Water, Sandalwood*, Valerian*, Ylang Ylang* *flower essence

🎯 Purpose 106 words ▾

Purpose Each dose contains equal parts of: Aesculus hippocastanum, flos (White Chestnut) 5X HPUS.........can't sleep because of thoughts going around in head Ferrum Phos 12X HPUS..........................................................restlessness and sleeplessness; anxious dreams Kali Carb 6C HPUS.................................................................agitated sleep; sleepless after 2 a.m. Kali Phos 6X HPUS................................................................sleeplessness from excessive mental exertion; worry over business troubles; from nervous exhauston Mag Phos 12X HPUS.............................................................sleep disturbed by troublesome dreams Nat Mur 6X HPUS..................................................................drowsiness during day; difficulty falling asleep; agitated sleep Populus termula, flos (Aspen) 5X HPUS...................................imagination runs wild Prunus cerasifera, flos (Cherry Plum) 5X HPUS........................feeling blocked or congested inside The letters HPUS indicate ingredients are in the Homeopathic Pharmacopoeia of the United States.

📋 Description 120 words ▾

Questions or Comments? Call 800.570.0021 Between 9am-5pm PST [email protected] siddhaflowers.com MFD by Siddha Flower Essences Oxnard, CA 93030 Made in USA

Side Panel homeopathy and flower essences: Jump start your body's natural ability to heal Natural, safe and non-habit forming No contraindications. May be effectively used with drugs and other supplements Alcohol, sugar, dairy and gluten free Prepared in purified water with natural preservatives Blends time-tested natural medicine with modern technology One month supply FOUNDATIONAL REMEDIES may be used with targeted remedies stress relief daily alignment emotional detox deep-seated stress TARGETED REMEDIES sleep male virility healthy hair blood sugar female balance lung and sinus muscles and joints throat and voice youthful skin teeth and gums happy heart hearing digestion sight

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breast-feeding ask a health professional before use

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children

📄 Package Label / Principal Display Panel 36 words ▾

Principal Display Panel 100% natural - no alcohol siddha cell salts + flower essences sleep Difficulty Falling Asleep Restless and Sleepless Agitated Sleep sugar, dairy and gluten free Homeopathic Remedy 1 US fl oz (29.6mL) Sleep

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

sleep Aesculus hippocastanum, flos, Ferrum Phos, Kali Carb, Kali Phos, Mag Phos, Nat Mur, Populus termula, flos, Prunus cerasifera, flos 5 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_C]/29.6mL; 6 [hp_X]/29.6mL; 12 [hp_X]/29.6mL; 6 [hp_X]/ SPRAY 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) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Siddha Flower Essences LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 bottle (69779-0012-01). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Siddha Flower Essences LLC 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.
← 69779-0011-01 · Siddha 69779-0013-01 · Siddha →
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.