ECZEMA REAL RELIEF- fumaria officinalis, natrum muriaticum, agaricus muscarius, petroleum, sepia, kali arsenicosum, alumina tablet, chewable
HOMEOLAB USA INC.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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DRUG FACTS

ACTIVE INGREDIENTS HPUS

Fumaria officinalis (Common fumitory) 6C

Natrum muriaticum (Salt) 6C

Agaricus muscarius (Fly agaric) 6C

Petroleum (Rock-oil) 6C

Sepia (Sepia) 6C

Kali arsenicosum (Potassium arsenite) 6C

Alumina (Alumina) 6C

The letters 'HPUS' indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

PURPOSE

dry scaly skin

dry and cracked skin, body rash

itching and redness

intense itching behind the ears, redness, dry and cracked skin

itching

dry skin and itching

itching rash

USES

This homeopathic medicine helps relieve symptoms of eczema:

- dry skin

- body rashes

- cracked skin

- itching

WARNINGS

Stop use and ask a doctorif symptoms worsen or persist for more than 7 days.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

DIRECTIONS

Chew tablets and let dissolve in mouth.

Do not use more than directed.

Do not take with food.

Repeat 3 times daily and reduce intake with improvement or as directed by a health professional.

Age	Dose
Adults and children 12 years of age and older	2 tablets
Children 2 to 11 years of age	1 tablet
Children under 2 years of age	Ask a doctor

OTHER INFORMATION

Store at room temperature (68 - 77F).

Do not use if seal is broken or missing.

INACTIVE INGREDIENTS

Lactose, magnesium stearate.

CARTON

image of carton label

ECZEMA REAL RELIEF
fumaria officinalis, natrum muriaticum, agaricus muscarius, petroleum, sepia, kali arsenicosum, alumina tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:60512-6009
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL) (FUMARIA OFFICINALIS FLOWERING TOP - UNII:VH659J61ZL)	FUMARIA OFFICINALIS FLOWERING TOP	6 [hp_C]
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CATION	6 [hp_C]
AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037) (AMANITA MUSCARIA FRUITING BODY - UNII:DIF093I037)	AMANITA MUSCARIA FRUITING BODY	6 [hp_C]
KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E)	KEROSENE	6 [hp_C]
SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2)	SEPIA OFFICINALIS JUICE	6 [hp_C]
POTASSIUM ARSENITE ANHYDROUS (UNII: BM2U42PAKI) (ARSENITE ION - UNII:N5509X556J)	ARSENITE ION	6 [hp_C]
ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933)	ALUMINUM OXIDE	6 [hp_C]

Ingredient Name	Strength
Inactive Ingredients
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	8mm
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:60512-6009-0	90 in 1 BOTTLE; Type 0: Not a Combination Product	07/25/2012	03/01/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		07/25/2012	03/01/2022

Labeler - HOMEOLAB USA INC. (202032533)

Name	Address	ID/FEI	Business Operations
Establishment
HOMEOLAB USA INC.		202032533	manufacture(60512-6009)

Revised: 12/2025

Document Id: 471f3917-49e9-55be-e063-6394a90a6b85

Set id: 000cf6bc-9e52-4261-9c73-4087c5ba1142

Version: 2

Effective Time: 20251229

HOMEOLAB USA INC.