DR. RECKEWEG R35 CHADONTIN COMBINATION PRODUCT- aconitum napellus 6x, bryonia 30x, calcarea carbonica 30x, chamomilla 4x, colocynthis 12x, ignatia amara 30x, staphysagria 8x liquid

DR. RECKEWEG R35 Chadontin by

Drug Labeling and Warnings

DR. RECKEWEG R35 Chadontin 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

Aconitum napellus 6X, Bryonia 30X, Calcarea carbonica 30X, Chamomilla 4X, Colocynthis 12X, Ignatia amara 30X, Staphysagria 8X, 1 g each in 10 g.

PURPOSE

Purpose

Relieves discomfort and pain associated with teething

INDICATIONS & USAGE

Uses

For the temporary relief of:

• Discomfort and pain associated with teething

WARNINGS

Warnings

Do not use

• if allergic to plants of the daisy (Asteraceae/Compositae) family.

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

5-10 drops in some water 3-6 times daily 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# 53346-1335-5

Dr. Reckeweg R35 Chadontin

Homeopathic preparation for the temporary relief of:

• Discomfort and pain associated with teething

Manufactured by:

Dr. Reckeweg Co. GmbH

D-64625 Bensheim

Germany

1.68 fl oz
(50 ml)

INGREDIENTS AND APPEARANCE

DR. RECKEWEG R35 CHADONTIN  COMBINATION PRODUCT
aconitum napellus 6x, bryonia 30x, calcarea carbonica 30x, chamomilla 4x, colocynthis 12x, ignatia amara 30x, staphysagria 8x liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53346-1335
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	6 [hp_X]  in 50 mL
BRYONIA DIOICA ROOT (UNII: 53UB5FH7CX) (BRYONIA CRETICA SUBSP. DIOICA ROOT - UNII:53UB5FH7CX)	BRYONIA DIOICA ROOT	30 [hp_X]  in 50 mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	30 [hp_X]  in 50 mL
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ)	MATRICARIA RECUTITA	4 [hp_X]  in 50 mL
CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (CITRULLUS COLOCYNTHIS FRUIT PULP - UNII:23H32AOH17)	CITRULLUS COLOCYNTHIS FRUIT PULP	12 [hp_X]  in 50 mL
STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (STRYCHNOS IGNATII SEED - UNII:1NM3M2487K)	STRYCHNOS IGNATII SEED	30 [hp_X]  in 50 mL
DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (DELPHINIUM STAPHISAGRIA SEED - UNII:00543AP1JV)	DELPHINIUM STAPHISAGRIA SEED	8 [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: 53346-1335-5	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(53346-1335)