HEARTBURN RELIEF- oyster shell calcium carbonate, crude, sodium phosphate, dibasic, heptahydrate, strychnos nux-vomica seed tabl

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

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Active ingredient:
Calcareacarbonica 15X, Natrumphosphoricum 12X, Nuxvomica 10X
Available from:
Similasan Corporation
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
stomach pain, cramps acid indigestion, heartburn heartburn, acid indigestion According to homeopathic principles, the active ingredients in this product temporarily relieve minor symptoms such as: • Acid Indigestion • Cramps
Authorization status:
unapproved homeopathic
Authorization number:
59262-605-30

HEARTBURN RELIEF- oyster shell calcium carbonate, crude, sodium phosphate, dibasic,

heptahydrate, strychnos nux-vomica seed tablet, orally disintegrating

Similasan Corporation

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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Heartburn Relief

Drug Facts

Active Ingredients

Calcarea carbonica 15X

Purpos e

stomach pain, cramps

Active Ingredients

Natrum phosphoricum 12X

Purpos e

acid indigestion, heartburn

Active Ingredients

Nux vomica 10X

Purpos e

heartburn, acid indigestion

Us es *

According to homeopathic principles, the active ingredients in this product temporarily relieve minor

symptoms such as:

Acid Indigestion

Cramps

Warnings

According to homeopathic principles, symptoms may temporarily worsen before improving (Initial

exacerbation of symptoms).

Do not exceed recommended dosage.

Not intended for children under 2.

Antacids may interact with certain prescription drugs. If you are presently taking a prescription drug,

do not take this product without checking with your physician or other health professional.

If pregnant, trying to get pregnant or breast feeding, ask a health professional before use.

Keep out of reach of children.

In case of accidental overdose, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if:

symptoms worsen or persist for more than 72 hours

Directions Adults and Children ages 2 and older:

Take 1 tablet every 4 hours, up to 6 times a day. Do not swallow tablets whole, but chew or allow to

dissolve in the mouth. Tablet may also be dissolved in a glass of water. Or use as directed by a licensed

health care professional.

Other Information

Active ingredients are manufactured according to homeopathic principles.

Inactive Ingredients

Lactose, Magnesium stearate

Ques tions ?

Reach our representatives at 1-800-240-9780 or getinfo@similasanusa.com. www.SimilasanUSA.com

*These statements are based upon traditional homeopathic principles. They have not been reviewed by

the Food and Drug Administration.

PRINCIPAL DISPLAY PANEL

NDC 59262-605-30

Similasan

Heartburn Relief

Nux Vomica Actives

60 Dissolvable Tablets

HEARTBURN RELIEF

oyster shell calcium carbonate, crude, sodium phosphate, dibasic, heptahydrate, strychnos nux-vomica seed tablet,

orally disintegrating

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:59 26 2-6 0 5

Route of Administration

ORAL

Similasan Corporation

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

15 [hp_X]

SO DIUM PHO SPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70 WT22SF4B)

(PHOSPHATE ION - UNII:NK0 8 V8 K8 HR)

SODIUM PHOSPHATE,

DIBASIC, HEPTAHYDRATE

12 [hp_X]

STRYCHNO S NUX-VO MICA SEED (UNII: 26 9 XH139 19 ) (STRYCHNOS NUX-VOMICA

SEED - UNII:26 9 XH139 19 )

STRYCHNOS NUX-VOMICA

SEED

10 [hp_X]

Inactive Ingredients

Ingredient Name

Stre ng th

LACTO SE (UNII: J2B2A4N9 8 G)

MAGNESIUM STEARATE (UNII: 70 0 9 7M6 I30 )

Product Characteristics

Color

WHITE

S core

no sco re

S hap e

ROUND

S iz e

8 mm

Flavor

Imprint Code

Contains

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:59 26 2-6 0 5-30

6 0 in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

0 2/0 1/20 17

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

UNAPPROVED HOMEOPATHIC

0 2/0 1/20 17

Labeler -

Similasan Corporation (111566530)

Revised: 12/2016

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