DR. RECKEWEG R10 KLIMAKTERAN COMBINATION PRODUCT- cimicifuga racemosa 6x, lachesis mutus 12x, sanguinaria canadensis 6x, sepia 6x, sulfuricum acidum 6x liquid

Dr. Reckeweg R10 Klimakteran by

Drug Labeling and Warnings

Dr. Reckeweg R10 Klimakteran by is a Homeopathic medication manufactured, distributed, or labeled by PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients

Cimicifuga racemosa 6X, Lachesis mutus 12X, Sanguinaria canadensis 6X, Sepia 6X, Sulphuricum acidum 6X, 1 g each in 10 g.

PURPOSE

Purpose

Relieves symptoms associated with menopause

INDICATIONS & USAGE

Uses

For the temporary relief of minor symptoms associated with menopause such as:

• Hot flashes
• Moodiness
• Irritability
  

WARNINGS

Warnings

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

If pregnant or breastfeeding, ask a health care professional before use.

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions
Adults: 10-15 drops 1-3 times daily;

acute cases: 10-15 drops 3-6 times daily in a little water or undiluted or as recommended.

OTHER SAFETY INFORMATION

Other information

• Tamper resistant: do not use if safety ring at base of cap is broken.
• Retain outer carton for full product Information.

INACTIVE INGREDIENT

Inactive ingredients

Ethanol, purified water.

QUESTIONS

Questions?

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

PRINCIPAL DISPLAY PANEL

NDC# 53346-1310-5

Dr. Reckeweg R10 Klimakteran

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

• Hot flashes
• Moodiness
• Irritability
  

Manufactured by:

Dr. Reckeweg Co. GmbH

D-64625 Bensheim

Germany

1.68 fl oz
(50 ml)

INGREDIENTS AND APPEARANCE

DR. RECKEWEG R10 KLIMAKTERAN  COMBINATION PRODUCT
cimicifuga racemosa 6x, lachesis mutus 12x, sanguinaria canadensis 6x, sepia 6x, sulfuricum acidum 6x liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53346-1310
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9)	BLACK COHOSH	6 [hp_X]  in 50 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	12 [hp_X]  in 50 mL
SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508)	SANGUINARIA CANADENSIS ROOT	6 [hp_X]  in 50 mL
SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2)	SEPIA OFFICINALIS JUICE	6 [hp_X]  in 50 mL
SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF)	SULFURIC ACID	6 [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: 53346-1310-5	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(53346-1310)