Home FDA labels 2b50dbc5-fefa-3296-e063-6294a90ac8c3 A-36 openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name A-36
Generic name BOS TAURUS ADRENAL GLAND, AGRIMONIA EUPATORIA, BELLIS PERENNIS, CAMPHOR (NATURAL), MATRICARIA CHAMOMILLA, EQUISETUM HYEMALE, FRAXINUS AMERICANA BARK, FORMICA RUFA, HISTAMINE DIHYDROCHLORIDE, IODINE, POTASSIUM DICHROMATE, CANIS LUPUS FAMILIARIS MILK, SODIUM CHLORIDE, ANEMONE PULSATILLA, SALIX NIGRA BARK, AND TOBACCO LEAF
Manufacturer DNA Labs, Inc.
Product type HUMAN OTC DRUG
SPL set ID 161c4738-9ead-4687-9f5a-029d5a496e07
SPL ID 2b50dbc5-fefa-3296-e063-6294a90ac8c3
Version 3
Effective date 2025-01-09
Source export date 2026-09-28
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:07:28 Harmonized routes table Harmonized routes SUBLINGUAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name A-36 openfda.brand_name generic name BOS TAURUS ADRENAL GLAND, AGRIMONIA EUPATORIA, BELLIS PERENNIS, CAMPHOR (NATURAL), MATRICARIA CHAMOMILLA, EQUISETUM HYEMALE, FRAXINUS AMERICANA BARK, FORMICA RUFA, HISTAMINE DIHYDROCHLORIDE, IODINE, POTASSIUM DICHROMATE, CANIS LUPUS FAMILIARIS MILK, SODIUM CHLORIDE, ANEMONE PULSATILLA, SALIX NIGRA BARK, AND TOBACCO LEAF openfda.generic_name manufacturer name DNA Labs, Inc. openfda.manufacturer_name ndc package 58264-0328-1 openfda.package_ndc ndc product 58264-0328 openfda.product_ndc ndc11 package 58264032801 derived:openfda.package_ndc spl id 2b50dbc5-fefa-3296-e063-6294a90ac8c3 id spl set id 161c4738-9ead-4687-9f5a-029d5a496e07 set_id unii 3POA0Q644U openfda.unii unii 0B24UR1O1S openfda.unii unii 2HU33I03UY openfda.unii unii G39P120JQT openfda.unii unii 6YR2608RSU openfda.unii unii 9679TC07X4 openfda.unii unii 451W47IQ8X openfda.unii unii 55H0W83JO5 openfda.unii unii EBU0U94820 openfda.unii unii N20HL7Q941 openfda.unii unii M2776SWB29 openfda.unii unii 59677RXH25 openfda.unii unii QU52J3A5B3 openfda.unii unii T4423S18FM openfda.unii unii G0R4UBI2ZZ openfda.unii unii I76KB35JEV openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings Warnings Use only if cap seal is unbroken. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of the reach of children.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.