OHM Drainage Lymphatic

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: OHM Drainage Lymphatic
Generic name: AESCULUS HIPP, APIS MEL, ARANEA, BARYTA CARB, EQUISETUM HYEM, FUCUS, FUMARIA, JUGLANS CIN, KALI IOD, KALI MUR, MYOSOTIS, NASTURTIUM, NAT SULPHURICUM, PHYTOLACCA, SARSAPARILLA, SCROPHULARA, SECALE, TEUCRIUM SCOR, THYROIDINUM, VIPERA.
Manufacturer: OHM PHARMA INC.
Product type: HUMAN OTC DRUG
SPL set ID: 8a89d255-ce6d-4b09-8335-8abcd0123d1d
SPL ID: d44b0fad-c077-e84a-e053-2995a90a68d9
Version: 4
Effective date: 2021-12-29
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:36

Harmonized routes table
Harmonized routes
TOPICAL

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 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		OHM Drainage Lymphatic	openfda.brand_name
generic name		AESCULUS HIPP, APIS MEL, ARANEA, BARYTA CARB, EQUISETUM HYEM, FUCUS, FUMARIA, JUGLANS CIN, KALI IOD, KALI MUR, MYOSOTIS, NASTURTIUM, NAT SULPHURICUM, PHYTOLACCA, SARSAPARILLA, SCROPHULARA, SECALE, TEUCRIUM SCOR, THYROIDINUM, VIPERA.	openfda.generic_name
manufacturer name		OHM PHARMA INC.	openfda.manufacturer_name
ndc	package	66096-695-10	openfda.package_ndc
ndc	product	66096-695	openfda.product_ndc
ndc11	package	66096069510	derived:openfda.package_ndc
spl id		d44b0fad-c077-e84a-e053-2995a90a68d9	id
spl set id		8a89d255-ce6d-4b09-8335-8abcd0123d1d	set_id
unii		48FZ1BHO18	openfda.unii
unii		11E6VI8VEG	openfda.unii
unii		0B4FDL9I6P	openfda.unii
unii		2H1576D5WG	openfda.unii
unii		0YPR65R21J	openfda.unii
unii		6P669D8HQ8	openfda.unii
unii		6T6CO7R3Z5	openfda.unii
unii		3C18L6RJAZ	openfda.unii
unii		0ORO6NCA4M	openfda.unii
unii		660YQ98I10	openfda.unii
unii		535G2ABX9M	openfda.unii
unii		59677RXH25	openfda.unii
unii		VH659J61ZL	openfda.unii
unii		1C4QK22F9J	openfda.unii
unii		YH89GMV676	openfda.unii
unii		7S82P3R43Z	openfda.unii
unii		LOK3I16O7G	openfda.unii
unii		C73BK97H5J	openfda.unii
unii		01G9XEA93N	openfda.unii
unii		7H443NUB2T	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: FOR TOPICAL USE ONLY. DO NOT APPLY TO BROKEN SKIN. IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. If symptoms worsen or persist for more than 5 days, discontinue use and contact a health care professional. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. KEEP OUT OF REACH OF CHILDREN.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.