BM Eczema Ointment

Manufacturer: BM Private Limited
Effective date: 2026-02-12
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 02:37:34

Label at a glance#

ProductBM Eczema

Active ingredientECHINACEA, UNSPECIFIED, GRAPHITE, CALENDULA OFFICINALIS FLOWERING TOP, SULFUR

Label structure9 sections

Storage and handling

Storage: Store in a cool, dry place below 30°C (86°F). Protect from direct sunlight.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients (Ref. stand.) Each 40gm contains: Calendula ∅ (HPUS) Echinacea ∅ (HPUS) Graphites 2X (HPUS) Sulphur 4X (HPUS)

INACTIVE INGREDIENT SECTION

CETOSTEARYL ALCOHOL, PARAFFIN OIL, WHITE SOFT PARAFFIN

INDICATIONS & USAGE SECTION

Uses*

Helps temporarily relieve: skin irritation, rash, redness, itching, dryness

OTC - PURPOSE SECTION

Active ingredients Purpose*

Calendula Ø (HPUS)..................skin irritation

Echinacea Ø (HPUS).................redness

Graphites 2X (HPUS).............dryness

Sulphur 4X (HPUS) …………. Itching & rash

WARNINGS SECTION

Warnings:

For external use only.

Avoid contact with eyes and mucous membranes.

Keep out of reach of children.

If you have severe symptoms, consult a doctor before use.

Do not use on deep and puncture wounds, severe burns, and infected skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings:

Keep out of reach of children.

STORAGE AND HANDLING SECTION

Storage:

Store in a cool, dry place below 30°C (86°F).

Protect from direct sunlight.

DOSAGE & ADMINISTRATION SECTION

Directions:

Use as directed.

Clean the affected area before application.

Apply a thin layer to the affected area, 2-3 times daily or as directed by a physician.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 1:

Eczema

Package 2: Tube

eczema ointment tube

Carton Box

eczema ointment box

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Data code	QR Code	BM Homoeopathic Pharmaceuticals Eczema (Ointment) 40gm Help support to relieve the symptoms of eczema and associated indications (For external use only) DRAP Mfg. Enl. # 0041, Prod. Enl. # 0041880976		Eczema.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85816-6022-1	BM Eczema	40 g in 1 JAR	OINTMENT	40		4
85816-6022-2	BM Eczema	40 g in 1 TUBE	OINTMENT	40		4

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

BM Eczema
Calendula, Echinacea, Graphite, Sulfur
ECHINACEA, UNSPECIFIED
GRAPHITE
CETOSTEARYL ALCOHOL
WHITE PETROLATUM
MINERAL OIL
CALENDULA OFFICINALIS FLOWERING TOP
SULFUR

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85816-6022	85816-6022-1, 85816-6022-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ECHINACEA, UNSPECIFIED	4N9P6CC1DX	ACTIB
GRAPHITE	4QQN74LH4O	ACTIB
CETOSTEARYL ALCOHOL	2DMT128M1S	IACT
WHITE PETROLATUM	B6E5W8RQJ4	IACT
MINERAL OIL	T5L8T28FGP	IACT
CALENDULA OFFICINALIS FLOWERING TOP	18E7415PXQ	ACTIB
SULFUR	70FD1KFU70	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
2	2025-12-03	monthly-update	2026-06-03 17:44:52
1	2025-06-27	full-release	2026-06-01 02:34:11

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
BM Eczema	CALENDULA, ECHINACEA, GRAPHITE, SULFUR	BM Private Limited	388ceb70-1de2-df89-e063-6294a90a3896	2026-02-12	Warnings	Exact identifier ndc (package): 85816-6022-1 ndc (package): 85816-6022-2 ndc (product): 85816-6022 ndc11 (package): 85816602202 ndc11 (package): 85816602201 spl id: 4aa03044-7ad2-45b6-e063-6394a90aef7d spl set id: 388ceb70-1de2-df89-e063-6294a90a3896

Reported adverse events (FAERS/openFDA)#

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