DUST MIX ANTIGEN- antimon tart, arsenicum alb, blatta or, bromium, calc carb, cimex, drosera, hepar sulph calc, ictodes foetida, lycopodium, phos, pulsatilla, silicea terra, tabacum fumus liquid

Dust Mix Antigen by

Drug Labeling and Warnings

Dust Mix Antigen by is a Homeopathic medication manufactured, distributed, or labeled by Natural Creations, Inc, OHM Pharma, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS - equal amounts of: Dust Mix Antigen 6C, 12C, 30C, Antimon Tart 30C, Arsenicum Alb 30C, Blatta Or 30C, Bromium 30C, Calc Carb 30C, Cimex 30C, Drosera 30C, Hepar Sulph Calc 30C, Ictodes Foetida 30C, Lycopodium 30C, Phos 30C, Pulsatilla 30C, Silicea Terra 30C, Tabacum Fumus 30C

INDICATIONS & USAGE

USES: Temporarily relieves symptoms associated with allergic responses to dust.**

PURPOSE

USES: Temporarily relieves symptoms associated with allergic responses to dust.**

DOSAGE & ADMINISTRATION

DIRECTIONS: Adults & children above 12 years: 10 drops orally or as directed by a health care professional.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

WARNINGS

WARNINGS:

• Consult a physician for use in children under 12 years of age.
• IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
• KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
• Do not use if TAMPER EVIDENT seal is broken or missing.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: Purified Water, Ethyl Alcohol USP

QUESTIONS

QUESTIONS & COMMENTS?

Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

REFERENCES

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

PRINCIPAL DISPLAY PANEL

NDC: 43406-0140-1

Dust Mix Antigen

HOMEOPATHIC

1 fl oz (30mL) / 20% Alcohol

INGREDIENTS AND APPEARANCE

DUST MIX ANTIGEN 
antimon tart, arsenicum alb, blatta or, bromium, calc carb, cimex, drosera, hepar sulph calc, ictodes foetida, lycopodium, phos, pulsatilla, silicea terra, tabacum fumus liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43406-0140
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5)	ANTIMONY POTASSIUM TARTRATE	30 [hp_C]  in 1 mL
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	30 [hp_C]  in 1 mL
BLATTA ORIENTALIS (UNII: 535787266D) (BLATTA ORIENTALIS - UNII:535787266D)	BLATTA ORIENTALIS	30 [hp_C]  in 1 mL
BROMINE (UNII: SBV4XY874G) (BROMINE - UNII:SBV4XY874G)	BROMINE	30 [hp_C]  in 1 mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	30 [hp_C]  in 1 mL
CIMEX LECTULARIUS (UNII: W66P4K3SGW) (CIMEX LECTULARIUS - UNII:W66P4K3SGW)	CIMEX LECTULARIUS	30 [hp_C]  in 1 mL
DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ)	DROSERA ROTUNDIFOLIA	30 [hp_C]  in 1 mL
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q)	CALCIUM SULFIDE	30 [hp_C]  in 1 mL
SYMPLOCARPUS FOETIDUS ROOT (UNII: R88254608W) (SYMPLOCARPUS FOETIDUS ROOT - UNII:R88254608W)	SYMPLOCARPUS FOETIDUS ROOT	30 [hp_C]  in 1 mL
LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479)	LYCOPODIUM CLAVATUM SPORE	30 [hp_C]  in 1 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	30 [hp_C]  in 1 mL
PULSATILLA VULGARIS (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV)	PULSATILLA VULGARIS	30 [hp_C]  in 1 mL
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	30 [hp_C]  in 1 mL
TOBACCO SMOKE (UNII: 9BPR10844H) (TOBACCO SMOKE - UNII:9BPR10844H)	TOBACCO SMOKE	30 [hp_C]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43406-0140-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	07/12/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		07/12/2012

Labeler - Natural Creations, Inc (018022074)

Establishment
Name	Address	ID/FEI	Business Operations
OHM Pharma, Inc		030572478	manufacture(43406-0140)