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Kids Relief PULSATILLA, ALLIUM CEPA, ARSENICUM ALBUM, NUX VOMICA, EUPHRASIA OFFINALIS, SABADILLA, STICTA PULMONARIA, ARAILA RACEMOSA, CUPRUM METALLICUM 8 [hp_X]/25mL; 6 [hp_X]/25mL; 8 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mL Liquid — NDC 71971-9077-08 package photo

Kids Relief PULSATILLA, ALLIUM CEPA, ARSENICUM ALBUM, NUX VOMICA, EUPHRASIA OFFINALIS, SABADILLA, STICTA PULMONARIA, ARAILA RACEMOSA, CUPRUM METALLICUM 8 [hp_X]/25mL; 6 [hp_X]/25mL; 8 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mL Liquid

by Homeolab International (Canada) inc · 1 BOTTLE in 1 CARTON (71971-9077-8) / 25 mL in 1 BOTTLE
NDC 71971-9077-08
🏷️ FDA NDC (as labeled) 71971-9077-8 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 17, 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

🆔 Identity & classification

FDA NDC (as labeled) 71971-9077-8
Product NDC 71971-9077
11-digit billing NDC 71971907708
UNII I76KB35JEV, 492225Q21H, S7V92P67HO, 269XH13919, C9642I91WL, 6NAF1689IO +3 more
UPC 0778159676390
SPL Set ID ba120c26-1e84-48b9-b38a-df5aa75ea6ce
Established class (EPC) Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Copper-containing Intrauterine Device
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production; Decreased Embryonic Implantation; Decreased Sperm Motility; Inhibit Ovum Fertilization
Chemical class Allergens; Dietary Proteins; Vegetable Proteins; Plant Proteins; Seed Storage Proteins; Copper
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-03-03
Route ORAL
Dosage form LIQUID
Substance ANEMONE PULSATILLA; ONION; ARSENIC TRIOXIDE; STRYCHNOS NUX-VOMICA SEED; EUPHRASIA STRICTA; SCHOENOCAULON OFFICINALE SEED; LOBARIA PULMONARIA; ARALIA RACEMOSA ROOT; COPPER
Why two NDCs? The FDA registers this code as 71971-9077-8 — a 5-4-1 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 package segment → 71971-9077-08. 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.

🏭 Manufacturer & labeler

LabelerHomeolab International (Canada) inc
Labeler code71971
First marketedMar 2017
Product typeHuman Otc Drug
Portfolio23 products on file
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.

🩺 Clinical

🧪 What is this product?

Kids Relief Pulsatilla is an unapproved homeopathic liquid taken by mouth that combines multiple plant and mineral substances. The product contains pulsatilla, onion, arsenicum, nux vomica, euphrasia, sabadilla, sticta pulmonaria, aralia racemosa, and copper in homeopathic potencies. In homeopathic practice, these ingredients are traditionally used to address symptoms like runny nose, sneezing, eye irritation, and cold-like complaints. Homeopathic products are marketed based on homeopathic tradition and have not been evaluated by the FDA 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.

🧪 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 DSO12WL7AU
    A salt derived from citric acid, this ingredient acts as a buffer and pH regulator in medicines. It helps maintain stable acidity levels and may improve taste or aid preservation.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 506T60A25R
    Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

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

The official label also statesInactive Ingredients Purified water, sorbitol, banana flavor, sodium benzoate, potassium sorbate, citric acid.

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.

💲 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.
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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Kids Relief 8 [hp_X]/25mL; 6 [hp_X]/25mL; 8 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mLthis 71971-9077-08 Homeolab 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

🏛️
2017
On the market since
Mar 2017
📍
2026
Currently FDA-listed
9 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
71971-9077-08 You're viewing this 1 BOTTLE in 1 CARTON (71971-9077-8) / 25 mL in 1 BOTTLE 2017-03-03 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Kids Relief PULSATILLA, ALLIUM CEPA, ARSENICUM ALBUM, NUX VOMICA, EUPHRASIA OFFINALIS, SABADILLA, STICTA PULMONARIA, ARAILA RACEMOSA, CUPRUM METALLICUM 8 [hp_X]/25mL; 6 [hp_X]/25mL; 8 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mL; 6 [hp_X]/25mL LIQUID 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 FDA registers it as 71971-9077-8, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 71971-9077-08, written without dashes as 71971907708. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 71971-9077-08, the first segment (71971) is the labeler code FDA assigned to Homeolab International (Canada) inc; the middle segment (9077) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (08) identifies this exact package size and type. Together they name one specific package of one specific product.
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 Homeolab International (Canada) inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Homeolab International (Canada) 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.

📄 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
🎯 Indications and Usage 27 words ▾

Uses This homeopathic medicine is made from a combination of ingredients traditionally used to help relieve allergy symptoms*: •sneezing •nasal congestion •throat and skin irritation •teary eyes

⏱️ Dosage and Administration 55 words ▾

Directions Children under 6 months of age : Consult a licensed healthcare practitioner before using this product Children under 6 months to 2 years old : 0.5 ml orally every 8 hours or 3 times a day Children 2 to 12 years old : 0.75 ml orally every 8 hours or 3 times a day

⚠️ Warnings 23 words ▾

Warnings Stop use and ask a doctor in cases of hgh fever or if symptoms worsen or persist for more than 2 days.

📦 Storage and Handling 17 words ▾

Other information •Store at room temperature • Do not use if bottle seal is broken or missing.

🧪 Active Ingredient 61 words ▾

Active Ingredients HPUS: Pulsatilla 8X (Wind flower) Allium cepa 6X (Onion) Arsenicum album 8X (Arsenous oxide) Nux Vomica 6X (Poison nut) Euphrasia officinalis 6X (Eyebright) Sabadilla 6X (Cevadilla) Sticta pulmonaria 6X (Lungwort) Aralia racemosa 6X (Spikenard) Cuprum metallicum 8X (Copper) The letters 'HPUS' indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.

🧪 Inactive Ingredients 13 words ▾

Inactive Ingredients Purified water, sorbitol, banana flavor, sodium benzoate, potassium sorbate, citric acid.

🎯 Purpose 69 words ▾

Purpose Pulsatilla 8X......................................nasal congestion, skin irritation (Wind flower) Allium cepa 6X (Onion)......................teary eyes Arsenicum album 8X..........................skin rash, throat irritation, sneezing (Arsenous oxide) Nux Vomica 6X..................................skin irritation, itchy nose and throat (Poison nut) Euphrasia officinalis 6X.......................eye and eyelid redness, burning tears (Eyebright) Sabadilla 6X (Cevadilla)......................wheezing, sneezing Sticta pulmonaria 6X...........................minor thorat irritation, runny nose (Lungwort) Aralia racemosa 6X (Spikenard)............frequent sneezing Cuprum metallicum 8X........................itching sensation of eyes, ears, throat and skin (Copper)

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 71971-9066-08 · Homeolab 71971-9083-08 · Homeolab →
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.