NUX MOSCHATA- nutmeg pellet

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

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Active ingredient:
NUTMEG (UNII: AEE24M3MQ9) (NUTMEG - UNII:AEE24M3MQ9)
Available from:
Boiron
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
Abdominal bloating accompanied by constipation* Stop use and ask a doctor if symptoms persist for more than 3 days or worsen
Authorization status:
unapproved medical gas
Authorization number:
0220-3698-41

NUX MOSCHATA- nutmeg pellet

Boiron

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been

approved by FDA. For further information about unapproved drugs, click here.

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Nux moschata 200CK

Nux moschata 200CK

(**contains 0.443 mg of the active ingredient per pellet)

Abdominal bloating accompanied by constipation*

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen

If pregnant or breast-feeding ask a health professional before use

Keep out of reach of children

Do not use if pellet dispenser seal is broken.

Contains approx 80 pellets.

How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully

remove the cap and use it to pour pellets under the tongue.

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL

EVIDENCE. NOT FDA EVALUATED.

*C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

lactose, sucrose

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until

symptoms are relieved or as directed by a doctor.

1-800-BOIRON-1 (1-800-264-7661),

BoironUSA.com Info@boiron.com

Distributed by Boiron, Inc. Newtown Square, PA 19073

NUX MOSCHATA

nutmeg pellet

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:0 220 -36 9 8

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

NUTMEG (UNII: AEE24M3MQ9 ) (NUTMEG - UNII:AEE24M3MQ9 )

NUTMEG

20 0 [kp_C] in 20 0 [kp_C]

Inactive Ingredients

Ingredient Name

Stre ng th

LACTO SE, UNSPECIFIED FO RM (UNII: J2B2A4N9 8 G)

SUCRO SE (UNII: C151H8 M554)

Product Characteristics

Color

white

S core

S hap e

ROUND

S iz e

Flavor

Imprint Code

Contains

Packag ing

Boiron

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:0 220 -36 9 8 -41 20 0 [kp_C] in 1 TUBE; Type 0 : No t a Co mbinatio n Pro duct

0 3/0 3/19 8 3

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved medical gas

0 3/0 3/19 8 3

Labeler -

Boiron (282560473)

Registrant -

Boiron, Inc. (014892269)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Bo iro n

28 256 0 473

ma nufa c ture (0 220 -36 9 8 )

Revised: 4/2019

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