![Poison Ivy Care Calendula officials, Stellaria media, St. Johns Wort, Rosemary Oil, Plantago major, Commiphora Myrrha, Comfrey Leaf, Salvia officinalis, Sunflower Oil 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_ Salve — NDC 70994-0204-09 package photo](https://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=480ee4ba-a92c-07ee-e054-00144ff8d46c&name=Poison_Ivy_Large_Hanger-O.jpg)
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Poison Ivy Care Calendula officials, Stellaria media, St. Johns Wort, Rosemary Oil, Plantago major, Commiphora Myrrha, Comfrey Leaf, Salvia officinalis, Sunflower Oil 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_ Salve — NDC 70994-204-09 (Billing 70994-0204-09)
by Spry Life LLC · 1 CAN in 1 BOX / 19 g in 1 CAN
This is a package of Poison Ivy Care Calendula officials, Stellaria media, St. Johns Wort, Rosemary Oil, Plantago major, Commiphora Myrrha, Comfrey Leaf, Salvia officinalis, Sunflower Oil 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_ Salve from Spry Life LLC, marketed since Apr 2016 and currently FDA-listed.
NDC 70994-0204-09
🏷️ FDA NDC (as labeled)
70994-204-09
billing pads the product segment with a zero
This package
Contains19 g in 1 can
Pack sizes3 compare ↓
🗂️ 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 →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
70994-204-09
Product NDC
70994-204
11-digit billing NDC
70994020409
UNII
YQR8R0SQEA, UFH8805FKA, 2H03479QVR, P0M7O4Y7YD, W2469WNO6U, UU81N77RI7 +2 more
SPL Set ID
480ee4ba-a92c-07ee-e054-00144ff8d46c
DEA schedule
Non-controlled
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2016-04-01
Route
TOPICAL
Dosage form
SALVE
Substance
ACHILLEA MILLEFOLIUM FLOWER; ST. JOHN'S WORT; STELLARIA MEDIA; CALENDULA OFFICINALIS FLOWER; PLANTAGO MAJOR; COMMIPHORA MYRRHA WHOLE; SALVIA OFFICINALIS WHOLE; COMFREY LEAF
Why two NDCs?
The FDA registers this code as 70994-204-09 — 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 → 70994-0204-09. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
Clinical
🧪 What is this product?
This is a topical salve marketed as a homeopathic product, containing multiple plant-derived ingredients including calendula flower, comfrey leaf, plantago, St. John's wort, yarrow flower, sage, myrrh, and chickweed. In homeopathic practice, these ingredients are traditionally used for skin concerns. Homeopathic products are marketed based on homeopathic tradition and are not evaluated by the FDA for effectiveness. This product is unapproved and is not supported by the same scientific evidence standards as FDA-approved medications.
Patient education
Supplement & herbal interactions
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about Calendula officials, Stellaria media, St. Johns Wort, Rosemary Oil, Plantago major, Commiphora Myrrha, Comfrey Leaf, Salvia officinalis, Sunflower Oil?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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 system | Per each | Per 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
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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 3, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 70994-0204-08 70994-204-08 Main listing | 113.4 g in 1 JAR | 2019-02-04 | — | Active |
| 70994-0204-09 You're viewing this | 1 CAN in 1 BOX / 19 g in 1 CAN | 2016-04-01 | — | Active |
| 70994-0204-10 70994-204-10 | 1 CAN in 1 BOX / 51.7 g in 1 CAN | 2016-04-01 | — | Active |
Pack size FAQ
What quantity is in this package?
This package is listed by the FDA — 1 can in 1 box / 19 g in 1 can.
What NDC number is used to bill for this package of Poison Ivy Care Calendula officials, Stellaria media, St. Johns Wort, Rosemary Oil, Plantago major, Commiphora Myrrha, Comfrey Leaf, Salvia officinalis, Sunflower Oil 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_ Salve?
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
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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2016
On the market since
Apr 2016
📍
2026
Currently FDA-listed
10 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.
- FDA Orange Book · refreshed Sep 3, 2026
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 H4N855PNZ1
Alpha-tocopherol is a form of vitamin E, a fat-soluble antioxidant derived from natural or synthetic sources. In medicines, it prevents oils and fats from breaking down and becoming rancid, protecting the product's stability and shelf life.
-
UNII C08B09D8UJ
Grindelia hirsutula is a plant-derived ingredient used as a natural flavoring agent or botanical extract in some formulations. It helps add flavor or plant-based characteristics to the medicine.
-
UNII 88N955S56P
A plant extract from Impatiens capensis (also called orange balsam). It may be used in formulations as a botanical ingredient, potentially serving roles such as a natural flavor, fragrance, or preservative component.
-
UNII PK0TXD049P
A plant extract from creosote bush leaves, used as a natural flavoring agent and preservative in some formulations. It may help maintain shelf stability and add taste to the medicine.
-
UNII ZBP1YXW0H8
A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
-
UNII 6UYK2W1W1E
A natural oil extracted from olives. It acts as an emollient and lubricant in formulations, helping to soften ingredients and improve how the medicine spreads or flows.
-
UNII 8LGU7VM393
Rosemary leaf oil is a natural aromatic oil extracted from rosemary plants. It's used in medicines as a flavoring agent and preservative to help protect the product from spoilage.
-
UNII FE663Z8IRO
A resinous gum extracted from the styrax tree, used as a preservative and binder in medicines. It helps prevent spoilage and holds ingredients together in solid formulations.
-
UNII 3W1JG795YI
Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
-
UNII 2ZA36H0S2V
Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.
10 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesOrganic Olea Europaea (Olive) Fruit Oil, Organic Helianthus Annuus (Sunflower) Seed Oil, Organic Cera Alba (Beeswax), Styrax Benzoin Gum, Larrea Tridentata (Chapparal) Extract, Tocopherol (Vitamin E), Lavandula Angustifolia (Lavender)Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Grindelia Camporum Flower/Leaf, Impatiens Capensis Extract.
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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
LabelerSpry Life LLC
Labeler code70994
First marketedApr 2016
Product typeHuman Otc Drug
Portfolio25 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
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
📄 Keep Out of Reach of Children
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Indications & Usage ■ temporarily protects minor ■ rashes ■ blisters ■ helps prevent and temporarily protects and helps relieve ■ cracked skin ■ temporarily protects and helps relieve minor skin irritation and itching due to ■ poison ivy ■ poison sumac ■ poison oak ■ temporarily protects and helps relieve minor pain associated with ■ poison ivy ■ poison sumac ■ poison oak
⏱️ Dosage and Administration ▾
Dosage & Administration Section Clean and dry skin. Apply as often as needed to affected area.
⚠️ Warnings ▾
Warnings Section Warnings For external use only. ■ Do not use on ■ on deep wounds ■ animal bites ■ serious burns ■ Stop use and ask a doctor if ■ condition worsens ■ symptoms last more than 7 days or clear up and occur again within a few days ■ When using this product keep out of eyes. Rinse with water to remove.
📦 Storage and Handling ▾
Storage Store at room temperature.
🧪 Active Ingredient ▾
Active Ingredients Organic Calendula Officinalis (Calendula) Flower Oil 1X (HPUS) Organic Plantago Major (Plantain) Leaf Extract 1X (HPUS) Organic Stellaria Media (Chickweed) Extract 1X (HPUS) Organic Symphytum Officinale (Comfrey) Leaf Powder 1X (HPUS) OrganicAchilleaMillefolium(Yarrow)Extract1X(HPUS) Commiphora Myrrha (Myrrh) Resin 1X (HPUS) Organic Salvia Officinalis (Sage) Leaf 1X (HPUS) Organic Hypericum Perforatum (St. John’s Wort) Oil 1X (HPUS)
🧪 Inactive Ingredients ▾
Inactive Ingredients Organic Olea Europaea (Olive) Fruit Oil, Organic Helianthus Annuus (Sunflower) Seed Oil, Organic Cera Alba (Beeswax), Styrax Benzoin Gum, Larrea Tridentata (Chapparal) Extract, Tocopherol (Vitamin E), Lavandula Angustifolia (Lavender)Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Grindelia Camporum Flower/Leaf, Impatiens Capensis Extract.
🎯 Purpose ▾
Purpose Section Skin Protectant Astringent External Analgesic
📄 Keep Out of Reach of Children ▾
Keep out of reach of children section Keep out of reach of children.
📄 Package Label / Principal Display Panel ▾
Principal Display Panel Poison Ivy
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Calendula officials, Stellaria media, St. Johns Wort, Rosemary Oil, Plantago major, Commiphora Myrrha, Comfrey Leaf, Salvia officinalis, Sunflower Oil — the ingredient across all brands.
Top reported reactions
Reporter sex
Male · 100%
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
About this NDC listing & data coverage
Over-the-counter (OTC) product
Homeopathic listing
About homeopathic listings
Poison Ivy Care Calendula officials, Stellaria media, St. Johns Wort, Rosemary Oil, Plantago major, Commiphora Myrrha, Comfrey Leaf, Salvia officinalis, Sunflower Oil 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_X]/51.7g; 1 [hp_ SALVE 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 Spry Life 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 2 other package presentations of this same product, including 1 can (70994-0204-10), 113.4 g (70994-0204-08). 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?
Spry Life 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.
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.