PREMIER VALUE SODIUM BICARBONATE- sodium bicarbonate powder

Land: Bandaríkin

Tungumál: enska

Heimild: NLM (National Library of Medicine)

Virkt innihaldsefni:

SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37)

Fáanlegur frá:

Chain Drug Consortium

INN (Alþjóðlegt nafn):

SODIUM BICARBONATE

Samsetning:

SODIUM BICARBONATE 1000 mg in 1 g

Stjórnsýsluleið:

ORAL

Gerð lyfseðils:

OTC DRUG

Ábendingar:

Antacid For relief of heartburn, acid indigestion, and upset stomach associated with these symptoms. you are currently taking a prescription drug. Antacids may interact with certain prescription drugs.

Leyfisstaða:

OTC monograph final

Vara einkenni

PREMIER VALUE SODIUM BICARBONATE- SODIUM BICARBONATE POWDER
CHAIN DRUG CONSORTIUM
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may be marketed if they_
_comply with applicable regulations and policies. FDA has not
evaluated whether this product complies._
----------
PREMIER VALUE SODIUM BICARBONATE
Drug Facts
ACTIVE INGREDIENT
Soduim Bicarbonate, USP
PURPOS E
Antacid
US E
For relief of heartburn, acid indigestion, and upset stomach
associated with these symptoms.
WARNINGS
NOT FOR INJECTIONS
Except under supervision of a doctor do not administer to children
under 6 years of age.
Do not take more than six, 1/2 tsp. per person up to 60 years old, or
three 1/2 tsp. per person 60 years or
older in a 24 hour period.
Do not use this product if you are on a sodium restricted diet (each
1/2 tsp. contains 30 mEq (0.7 g)
Sodium).
Do not use the maximum does more than 2 weeks.
ASK A DOCTOR OR PHARMACIST BEFORE USE IF
you are currently taking a prescription drug. Antacids may interact
with certain prescription drugs.
KEEP OUT OF REACH OF CHILDREN.
In case of accidental overdose, seek professional assistance or
contact a Poison Control Center
immediately.
DIRECTIONS
Adult and children 6 yrs of age and older:
Take 1/2 tsp. in 1/2 g;ass (4 fl oz) of water every 2 hrs. up to
maximum dosage or as directed by doctor.
INACTIVE INGREDIENTS
none
LABEL
PREMIER VALUE SODIUM BICARBONATE
sodium bicarbonate powder
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 8 0 16 -6 8 5
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
SO DIUM BICARBO NATE (UNII: 8 MDF5V39 QO) (SODIUM CATION - UNII:LYR4M0
NH37)
SODIUM BICARBONATE 10 0 0 mg in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:6 8 0 16 -6 8 5-
0 1
454 g in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n
Pro duc t
10 /27/20 17
2
NDC:6 8 0 16 -6 8 5-
9 4