PERTUSSINUM- NOSODE liquid

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

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Active ingredient:
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN) (HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED - UNII:U364V64HUN)
Available from:
Newton Laboratories, Inc.
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
Law of similars; Spasmatic coughing attacks Law of similars; Spasmatic coughing attacks
Authorization status:
unapproved homeopathic
Authorization number:
55714-6495-1

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PERTUSSINUM (NOSODE)- pertussinum (nosode) liquid

Newton Laboratories, Inc.

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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Pertussinum 6495L

INDICATIONS & USAGE SECTION

Law of similars; Spasmatic coughing attacks

DOSAGE & ADMINISTRATION SECTION

Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) as needed or as directed by a health

professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Pertussinum 200c, Pertussinum 30c

OTC - PURPOSE SECTION

Law of similars; Spasmatic coughing attacks

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

QUESTIONS SECTION

newtonlabs.net - Questions? 1.800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

WARNINGS SECTION

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing.

If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-

feeding, ask a doctor before use.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PERTUSSINUM (NOSODE)

pertussinum (nosode) liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:55714-6 49 5

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

HUMAN SPUTUM, BO RDETELLA PERTUSSIS INFECTED (UNII: U36 4V6 4HUN)

(HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED - UNII:U36 4V6 4HUN)

HUMAN SPUTUM,

BORDETELLA PERTUSSIS

INFECTED

30 [hp_C]

in 1 mL

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

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

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:55714-

6 49 5-1

29 .57 mL in 1 BOTTLE, GLASS; Type 0 : No t a Co mbinatio n

Pro duc t

0 8 /0 1/20 11

Newton Laboratories, Inc.

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 8 /0 1/20 11

Labeler -

Newton Laboratories, Inc. (788793610)

Registrant -

Newton Laboratories, Inc. (788793610)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Newto n Labo rato ries, Inc.

78 8 79 36 10

ma nufa c ture (55714-6 49 5)

Revised: 12/2020

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