SAL DE UVAS PICOT- citric acid monohydrate and sodium bicarbonate granule, effervescent

Sal de Uvas Picot by

Drug Labeling and Warnings

Sal de Uvas Picot by is a Otc medication manufactured, distributed, or labeled by Reckitt Benckiser Mexico, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients (in each packet)	Purposes
Citric acid 1.9485 g	Antacid
Sodium bicarbonate (heat-treated) 2.4850 g	Antacid

Uses

for the relief of

• heartburn
• sour stomach
• acid indigestion
• upset stomach associated with these symptoms

Warnings

Do not take more than directed or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a physician.

Ask a doctor before use if you have a sodium-restricted diet.

Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.

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

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center immediately.

Directions

• fully dissolve one packet in ½ glass of water every 4 hours or as directed by a doctor
• adults 60 years of age and over: do not exceed 3 packets in 24 hours
• adults and children 12 to 60 years of age: do not exceed 4 packets in 24 hours
• children under 12 years of age: ask a doctor

Other information

• each packet contains: sodium 712 mg
• store in a cool, dry place
• store between 20-25ºC (68-77ºF)

Inactive ingredients

silicon dioxide, sucrose, tartaric acid

Questions ?

1-844-700-9956

PRINCIPAL DISPLAY PANEL - 12 Packet Carton

UPSET
STOMACH

sal de uvas
picot®

12 packets

Citric AcidAntacid
Sodium BicarbonateAntacid
Effervescent Powder for Solution

INGREDIENTS AND APPEARANCE

SAL DE UVAS PICOT 
citric acid monohydrate and sodium bicarbonate granule, effervescent

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70565-580
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Citric Acid monohydrate (UNII: 2968PHW8QP) (Anhydrous Citric Acid - UNII:XF417D3PSL)	Anhydrous Citric Acid	1.9485 g
Sodium Bicarbonate (UNII: 8MDF5V39QO) (Sodium Cation - UNII:LYR4M0NH37, Bicarbonate Ion - UNII:HN1ZRA3Q20)	Sodium Bicarbonate	2.485 g

Inactive Ingredients
Ingredient Name	Strength
Silicon dioxide (UNII: ETJ7Z6XBU4)
Sucrose (UNII: C151H8M554)
Tartaric acid (UNII: W4888I119H)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70565-580-01	6 in 1 CARTON	03/31/2016
1		1 in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 70565-580-02	8 in 1 CARTON	03/31/2016
2		1 in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 70565-580-03	12 in 1 CARTON	03/31/2016
3		1 in 1 PACKET; Type 0: Not a Combination Product
4	NDC: 70565-580-04	50 in 1 CARTON	03/31/2016
4		1 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 FINAL	part331	03/31/2016

Labeler - Reckitt Benckiser Mexico, S.A. de C.V. (810061093)