RESPIRO-PRO T016 (ammonium muriaticum, antimonium tartaricum, arsenicum album, bryonia- alba, calcarea carbonica, lobelia inflata, natrum sulphuricum, phosphorus, spongia tosta liquid

Respiro-Pro by

Drug Labeling and Warnings

Respiro-Pro by is a Homeopathic medication manufactured, distributed, or labeled by Guangzhou Renuma Medical Systems Co., Ltd, Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Ammonium Muriaticum 30X, Antimonium Tartaricum 30X, Arsenicum Album 30X, Bryonia (Alba) 30X, Calcarea Carbonica 30X, Lobelia Inflata 30X, Natrum Sulphuricum 30X, Phosphorus 30X, Spongia Tosta 30X.

INDICATIONS:

May temporarily relieve symptoms due to chronic lung disorders, lung inflammation.

WARNINGS:

If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Do not use if tamper evident seal is broken or missing.
Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional.
Consult a physician for use in children under 12 years of age.

INDICATIONS:

May temporarily relieve symptoms due to chronic lung disorders, lung inflammation.

INACTIVE INGREDIENTS:

Demineralized water, Glycerin

QUESTIONS:

Distributed by:
Guangzhou Renuma Medical
Systems Co., Ltd.
No. 5, 2nd Floor, Ascendas 2nd Street
Sino-Singapore Guangzhou Knowledge City
Guangzhou 510555, China

PACKAGE LABEL DISPLAY:

RESPIRO-PRO
T016
HOMEOPATHIC
2 fl. oz. (59 ml)

INGREDIENTS AND APPEARANCE

RESPIRO-PRO  T016
ammonium muriaticum, antimonium tartaricum, arsenicum album, bryonia (alba), calcarea carbonica, lobelia inflata, natrum sulphuricum, phosphorus, spongia tosta liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71742-0010
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4)	AMMONIUM CATION	30 [hp_X]  in 1 mL
ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5)	ANTIMONY POTASSIUM TARTRATE	30 [hp_X]  in 1 mL
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	30 [hp_X]  in 1 mL
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	30 [hp_X]  in 1 mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	30 [hp_X]  in 1 mL
LOBELIA INFLATA (UNII: 9PP1T3TC5U) (LOBELIA INFLATA - UNII:9PP1T3TC5U)	LOBELIA INFLATA	30 [hp_X]  in 1 mL
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750)	SODIUM SULFATE	30 [hp_X]  in 1 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	30 [hp_X]  in 1 mL
SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID)	SPONGIA OFFICINALIS SKELETON, ROASTED	30 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71742-0010-1	59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	10/26/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/26/2017

Labeler - Guangzhou Renuma Medical Systems Co., Ltd (544538706)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(71742-0010) , api manufacture(71742-0010) , label(71742-0010) , pack(71742-0010)