DR. SANA ALIVIO DIGESTIVO UPSET STOMACH- efefervescent antacid granule, effervescent

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredients

Sodium bicarbonate 2,485 mg

Purpose

Antacid

Uses

For relief of heartburn, acid indigestion, and upset stomach associated with these symptoms.

Warning

STOMACH WARNING: To avoid serious injury, do not take until powder is completely dissolved. It is very important not to take this product when overly full from food or drink. Consult a doctor if severe stomach pain occurs after taking this product.

Do not use

If you are on a sodium-restricted diet unless directed by a doctor
If you have kidney disease, unless directed by a doctor

Ask a Doctor before use

Ask a doctor before use if you have:

• Heart disease
• High blood pressure
• Kidney disease
• A sodium-restricted diet

When using

Do not take more than 6 packets in 24 hours if you are between 12 and 60 years old, and 3 packets in 24 hours if you are over 60 years old or do not use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a physician.

Stop Use

STOP USE AND ASK A DOCTOR IF

• symptoms persist
• symptoms worsen
• You experience severe stomach pain
• If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

Keep out of reach of children.

Directions

Adults and children 12 years and over: dissolve one packet in ½ glass (4 fl oz) of water every 4 hours or as directed by a doctor. Adults and children 12 to 60 years of age; do not exceed 6 packets in 24 hours. Adults 60 years of age and over, do not exceed 3 packets in 24 hours. Children under 12 years of age: do not use.

Other Information

Each packet contains: sodium 712 mg.
store in a cool, dry place at 20°–25°C (68°–77°F)

Inactive Ingredients

Citric acid, tartaric acid, sucrose, and silicon dioxide

Display panel packet

Display panel Box

INGREDIENTS AND APPEARANCE

DR. SANA ALIVIO DIGESTIVO  UPSET STOMACH
efefervescent antacid granule, effervescent

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84178-110
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BICARBONATE ION (UNII: HN1ZRA3Q20) (SODIUM CATION - UNII:LYR4M0NH37)	BICARBONATE ION	2485 mg  in 5000 mg

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	1948.5 mg  in 5000 mg
SUCROSE (UNII: C151H8M554)	316.5 mg  in 5000 mg
TARTARIC ACID (UNII: W4888I119H)	200 mg  in 5000 mg
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)	50 mg  in 5000 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84178-110-01	12 in 1 BOX	05/13/2026
1		5000 mg in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	05/13/2026

Labeler - EVI LABS (123617598)

Establishment
Name	Address	ID/FEI	Business Operations
EVI LABS		123617598	manufacture(84178-110)