DR. RECKEWEG R59 VESICULINE COMBINATION PRODUCT- calcarea carbonica 12x, fucus vesiculosus 4x, graphites 12x, natrum sulphuricum

United States - English - NLM (National Library of Medicine)

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Active ingredient:
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I), FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M), GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O), SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750), SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID)
Available from:
PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO
INN (International Name):
OYSTER SHELL CALCIUM CARBONATE, CRUDE
Composition:
OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X] in 50 mL
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
Purpose Relieves symptoms associated with weight gain due to glandular dysfunction Uses For the temporary relief of minor symptoms associated with: - Weight gain due to glandular dysfunction
Authorization status:
unapproved homeopathic
Authorization number:
53346-1359-5

DR. RECKEWEG R59 VESICULINE COMBINATION PRODUCT- calcarea carbonica 12x,

fucus vesiculosus 4x, graphites 12x, natrum sulphuricum 4x, spongia tosta 4x liquid

PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO

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.

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DR. RECKEWEG R59 Vesiculine

Active ingredients

Calcarea carbonica 12X, Fucus vesiculosus 4X, Graphites 12X, Natrum sulphuricum 4X, Spongia tosta

4X, 1 g each in 10 g.

Purpos e

Relieves symptoms associated with weight gain due to glandular dysfunction

Us es

For the temporary relief of minor symptoms associated with:

Weight gain due to glandular dysfunction

Warnings

Do not use

if you are hypersensitive to iodine

if you have a thyroid condition (e.g. hypothyroidism or hyperthyroidism)

if you are pregnant or breastfeeding

in cases with intestinal affections

Stop use and ask a doctor if symptoms persist, get worse, or if new symptoms occur.

Keep out of reach of children.

Directions

Adults and children ≥ 12 years 5-10 drops 1-3 times daily in a little water or undiluted or as

recommended.

Other information

Tamper resistant: do not use if safety ring at base of cap is broken.

Retain outer carton for full product instructions.

Inactive ingredients

Ethanol, purified water.

Ques tions ?

Call 1-800-361-7872 or email questions@reckeweg.com

NDC# 53346-1359-5

Dr. Reckeweg R59 Vesiculine

Homeopathic preparation for the temporary relief of minor symptoms associated with:

Weight gain due to glandular dysfunction

Manufactured by:

Dr. Reckeweg Co. GmbH

D-64625 Bensheim

Germany

1.68 fl oz

(50 ml)

DR. RECKEWEG R59 VESICULINE COMBINATION PRODUCT

calcarea carbonica 12x, fucus vesiculosus 4 x, graphites 12x, natrum sulphuricum 4 x, spongia tosta 4 x liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:53346 -1359

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

O YSTER SHELL CALCIUM CARBO NATE, CRUDE (UNII: 2E328 21G6 I) (OYSTER

SHELL CALCIUM CARBONATE, CRUDE - UNII:2E328 21G6 I)

OYSTER SHELL CALCIUM

CARBONATE, CRUDE

12 [hp_X]

in 50 mL

FUCUS VESICULO SUS (UNII: 535G2ABX9 M) (FUCUS VESICULOSUS -

UNII:535G2ABX9 M)

FUCUS VESICULOSUS

4 [hp_X]

in 50 mL

GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O)

GRAPHITE

12 [hp_X]

in 50 mL

SO DIUM SULFATE (UNII: 0 YPR6 5R21J) (SODIUM SULFATE ANHYDROUS -

UNII:36 KCS0 R750 )

SODIUM SULFATE

4 [hp_X]

in 50 mL

SPO NGIA O FFICINALIS SKELETO N, RO ASTED (UNII: 1PIP39 4IID) (SPONGIA

OFFICINALIS SKELETON, ROASTED - UNII:1PIP39 4IID)

SPONGIA OFFICINALIS

SKELETON, ROASTED

4 [hp_X]

in 50 mL

Inactive Ingredients

Ingredient Name

Stre ng th

ALCO HO L (UNII: 3K9 9 58 V9 0 M)

WATER (UNII: 0 59 QF0 KO0 R)

PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:53346 -1359 -5

50 mL in 1 BOTTLE

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved ho meo pathic

0 6 /0 1/19 8 6

Labeler -

PHARMAZEUT ISCHE FABRIK DR. RECKEWEG & CO (318602612)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO

318 6 0 26 12

ma nufa c ture (53346 -1359 )

Revised: 4/2013

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