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P19 Collection/Guide/العربية

P19 · Reference page 14

Research and Product Records: Source Index

Editorial review: Moxa Sourcing ·

Every factual statement in this collection is tied to one of the records below. The index exists so that a reader can check the wording, the date and the read state, and so that a future editor can see what was actually opened rather than what was merely found.

1. Read states used in this collection

  • Full page read. The public page was read in full on 2026-11-13, and the statements attributed to it come from that reading.
  • Abstract read; full text not reviewed. The summary was read; the article body was not.
  • Lead only. A search result or citation was seen, but the underlying document was not opened.
  • Metadata and headings only. The page title, URL and stated role were used; the body was not re-read for this package.

These states are not interchangeable. A claim supported by an abstract is weaker than one supported by a full text, and a lead is not support at all.

2. Product listings

All six were read in full on 2026-11-13. They are public product pages derived from manufacturer materials; they are not test reports or certificates. Codes in brackets are the citation keys used in the chapters.

Each has a documented limitation. MS-CAT-29D5D09B3B does not state species, part or strength. MS-CAT-75A3663FE7 contains a material field (“mugwort”) that its own ingredient declaration does not support, and gives no roll-on formula. MS-CAT-04321578D7 carries two conflicting direction panels. MS-CAT-ADBE39E4F2 carries conflicting heating and weight fields. MS-CAT-49819BAC9D combines a not-self-heating field with warm-moxibustion language and a shared pouch. MS-CAT-0C0A4A2DC9 states no shelf life and uses a product name that is not a mechanism. The chapters preserve these limitations rather than resolving them by assumption.

3. Discussion records

Six public discussion records were read on 2026-11-13. None is a verified buyer, a clinical case or a demand estimate. Two relate directly to mugwort (D05 and P19Q01); four are adjacent.

4. External records

  • [K01] FDA National Drug Code Directory. fda.gov — National Drug Code Directory. Original page read. A directory of listings, not an approval or efficacy record.
  • [K02] DailyMed, “Mugwort Pain Relief Patch” label archive. dailymed.nlm.nih.gov. Original page read. A submitted label; the page shows an inactive code; not an endorsement.
  • [K03] Basiri Z, Zeraati F, Esna-Ashari F, et al. Topical effects of Artemisia absinthium ointment and liniment compared with piroxicam gel in knee osteoarthritis: a randomised double-blind controlled trial. Iranian Journal of Medical Sciences 2017;42(6):524–531. PMID 29184260; PMC5684373. pubmed.ncbi.nlm.nih.gov/29184260/. Abstract read via Europe PMC; full text not reviewed.
  • [K05] ISO 16128-1:2016, Guidelines on technical definitions and criteria for natural and organic cosmetic ingredients and products — Part 1: Definitions for ingredients. iso.org/standard/62503.html. Official abstract read; full standard not acquired. Scope is ingredient definitions; the abstract states that it does not address claims, labelling, safety, packaging or regulatory requirements.
  • [K06] U.S. Food and Drug Administration, “Organic” Cosmetics. fda.gov/cosmetics/cosmetics-labeling-claims/organic-cosmetics. Full page read. States that FDA has no definition of “organic” for cosmetics, that USDA NOP defines and certifies organic agricultural ingredients and labelling percentages, and that organic claims must comply with both USDA and FDA requirements.
  • [K04] FDA pharmacovigilance review of a topical analgesic patch (2016). fda.gov/media/100045/download. Lead only; full PDF not reviewed. A specific product and historical review, not a general safety standard.

5. Cross-topic method pages

These pages were not re-read in full for this package. Their titles, URLs and stated roles were used, and no parameters were migrated from them into P19.

6. What is not in this index

  • No mugwort pain-spray product file was located.
  • No direct question about a mugwort pain spray was located.
  • K03 was read in full through PubMed Central; K04 remains a lead. The ISO 16128-1 full standard was not acquired; only its official abstract was read.
  • No certification, test report or batch record for any of the six listings was available.
  • No search-volume, AI-citation or commercial outcome data was observed.

Those absences define the limits of the collection. They are recorded here so that a reader does not have to infer them from what is missing.

7. Technical and safety sources

The following sources support the linked explanations within their stated scopes. Capturing a document is not the same as reviewing all its sections; the read extent is recorded for each source.

K27 — 7 CFR 205.207. US wild-crop organic harvesting rule; no reference-product claim verified.

K28 — EMA GACP 2025 final. Herbal starting materials for herbal medicinal products; sections 2–14 read; no reference chain audited.

K29 — FDA Q3 2026 final. Topical drug ANDAs; sections I–IV read; not Q3 quality-control guidance or a classification/BE decision for reference products.

K30 — EMA herbal specifications Rev.3 (2022). Selected identity, assay, reference-material and impurity sections; medicinal scope.

K31 — FDA adhesion guidance (July 2026 final). ANDA medicinal systems; sections I–V and original scale reviewed.

K32 — FDA irritation/sensitization (July 2026 revised draft). Not for implementation; selected study-purpose, conduct and adverse-event sections.

K33 — FDA BAM Chapter23 (July 2024). Cosmetics methods, selected sample handling/preparation and findings/preservation; no reference classification.

K34 — FDA Botanical Drug Development (2016 final). Selected scientific consistency, prior-experience, clinical-batch and analytical sections; not a current market-entry legal summary.

Source K35 — residual drug in medicinal delivery systems

2011 final guidance; sections I–IV read. Scientific interpretation of residual material and design justification; no reference-product measurement, safety rate, dose or disposal method established.
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