Label: DR. RECKEWEG R1 ANGINACID COMBINATION PRODUCT- apis mellifica 4x, baryta muriatica 6x, belladonna 4x, calcarea iodata 4x, hepar sulphuris calcareum 12x, kali bichromicum 4x, lachesis mutus 12x, teucrium marum 6x, mercurius corrosivus 6x, phytolacca decandra 4x liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 53346-1301-5 - Packager: PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO
- 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 April 9, 2013
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings
When using this product
- In very rare cases, skin reactions may occur after use.
- In these cases discontinue use of product.
- In rare cases, hypersalivation may occur after administration.
- In these cases discontinue use of product.
Stop use and ask a doctor if
- pain persists for more than one week (5 days in children)
- fever persists for more than 3 days
- symptoms worsen
- new symptoms occur
- redness or swelling is present
- sore throat is severe and persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting
Directions
Adults and children ≥ 12 years 5-10 drops; children (6-11 years) 3-5 drops;
children (2-5 years) 2-3 drops, all ages take 2-3 times daily in a little water or undiluted or as recommended.
In acute cases (see age group) the same dosage up to 6 times per day.
Not recommended for children under 2 years of age except under the advice of a health care professional.
- In very rare cases, skin reactions may occur after use.
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR. RECKEWEG R1 ANGINACID COMBINATION PRODUCT
apis mellifica 4x, baryta muriatica 6x, belladonna 4x, calcarea iodata 4x, hepar sulphuris calcareum 12x, kali bichromicum 4x, lachesis mutus 12x, teucrium marum 6x, mercurius corrosivus 6x, phytolacca decandra 4x liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53346-1301 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 4 [hp_X] in 50 mL BARIUM CHLORIDE DIHYDRATE (UNII: EL5GJ3U77E) (BARIUM CATION - UNII:V645272HLN) BARIUM CHLORIDE DIHYDRATE 6 [hp_X] in 50 mL ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 4 [hp_X] in 50 mL CALCIUM IODIDE (UNII: 8EKI9QEE2H) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM IODIDE 4 [hp_X] in 50 mL CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 12 [hp_X] in 50 mL POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 4 [hp_X] in 50 mL LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 12 [hp_X] in 50 mL TEUCRIUM MARUM (UNII: 10464S0TAA) (TEUCRIUM MARUM - UNII:10464S0TAA) TEUCRIUM MARUM 6 [hp_X] in 50 mL MERCURIC CHLORIDE (UNII: 53GH7MZT1R) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC CHLORIDE 6 [hp_X] in 50 mL PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG) PHYTOLACCA AMERICANA ROOT 4 [hp_X] in 50 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:53346-1301-5 50 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/01/1986 Labeler - PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO (318602612) Establishment Name Address ID/FEI Business Operations PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO 318602612 manufacture(53346-1301)