Label: ASTHMA DROPS 2010- asthma drops liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63083-2010-2 - Packager: Professional Complementary Health Formulas
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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.
Drug Label Information
Updated August 15, 2019
If you are a consumer or patient please visit this version.
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- ACTIVE INGREDIENTS
- QUESTIONS
- INDICATIONS
- PURPOSE
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WARNINGS
A persistent cough or chest pain may be signs of a serious condition. Consult a doctor promptly if symptoms persist. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.
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DIRECTIONS
Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day for up to 6 weeks. For immediate onset of symptoms, take 10 to 15 drops every 15 minutes up to 3 hours. For less severe symptoms, take 10-15 drops hourly up to 8 hours. Consult a physician for use in children under 12 years of age.
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- LABEL
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INGREDIENTS AND APPEARANCE
ASTHMA DROPS 2010
asthma drops liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63083-2010 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (ARALIA RACEMOSA ROOT - UNII:T90W4582DU) ARALIA RACEMOSA ROOT 3 [hp_X] in 59 mL LOBELIA CARDINALIS WHOLE (UNII: GT0PJ8MB5R) (LOBELIA CARDINALIS WHOLE - UNII:GT0PJ8MB5R) LOBELIA CARDINALIS WHOLE 3 [hp_X] in 59 mL SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED 3 [hp_X] in 59 mL ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE 8 [hp_X] in 59 mL ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (ACONITUM NAPELLUS WHOLE - UNII:U0NQ8555JD) ACONITUM NAPELLUS WHOLE 6 [hp_X] in 59 mL SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND 6 [hp_X] in 59 mL BLATTA ORIENTALIS (UNII: 535787266D) (BLATTA ORIENTALIS - UNII:535787266D) BLATTA ORIENTALIS 6 [hp_X] in 59 mL COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER 6 [hp_X] in 59 mL IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 6 [hp_X] in 59 mL IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC 6 [hp_X] in 59 mL LOBELIA INFLATA WHOLE (UNII: 9PP1T3TC5U) (LOBELIA INFLATA WHOLE - UNII:9PP1T3TC5U) LOBELIA INFLATA WHOLE 6 [hp_X] in 59 mL BEEF LUNG (UNII: 2I1RTO1MBR) (BEEF LUNG - UNII:2I1RTO1MBR) BEEF LUNG 6 [hp_X] in 59 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 12 [hp_X] in 59 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 12 [hp_X] in 59 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X] in 59 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63083-2010-2 59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/15/1985 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/15/1984 Labeler - Professional Complementary Health Formulas (167339027) Registrant - Natural Pharmaceutical Manufacturing LLC (015624923) Establishment Name Address ID/FEI Business Operations Natural Pharmaceutical Manufacturing LLC 015624923 manufacture(63083-2010)