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

ECZEMA by

Drug Labeling and Warnings

ECZEMA by is a Homeopathic medication manufactured, distributed, or labeled by HOMEOLAB USA INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

REFERENCES

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 doctor if 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

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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 VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037) (AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY - UNII:DIF093I037)	AMANITA MUSCARIA VAR. 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]

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60512-6009-0	90 in 1 BOTTLE

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

Labeler - HOMEOLAB USA INC. (202032533)

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