NDC | 47682-135-20, 47682-135-24, 47682-135-60 |
Set ID | 528da9d9-2a52-4c16-b7b2-61b3eee1abea |
Category | HUMAN OTC DRUG LABEL |
Packager | Unifirst First Aid Corporation |
Generic Name | |
Product Class | Anti-coagulant |
Product Number | |
Application Number | PART343 |
- Drug Facts
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Reye's syndrome:
Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.
Allergy alert:
Aspirin may cause a severe allergic reaction which may include:
- hives
- facial swelling
- asthma (wheezing)
- shock
If an allergic reaction occurs, stop use and seek medical help right away.
Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you:
- are age 60 or older
- have had stomach ulcers or bleeding problems
- take a blood thinning (anticoagulant) or steroid drug
- take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
- have 3 or more alcohol drinks every day while using this product
- take more or for a longer time than directed
Do not use
- if you have ever had an allergic reaction to any other pain reliever/ fever reducer
- if you are taking a prescription drug for gout, diabetes or arthritis
Ask a doctor before use if
- stomach bleeding warning applies to you
- you have a history of stomach problems such as heartburn
- you have high blood pressure, heart disease, liver cirrhosis, or kidney disease
- you are taking a diuretic
- you reached age 60 or older
- you are on a sodium restricted diet
Ask a doctor or pharmacist before use if you are
- taking any other drugs (prescription or non-prescription). Antacids may interact with certain drugs.
- under a doctor's care for any serious condition
When using this product do not exceed recommended dosage.
Stop use and ask a doctor if
- you experience any of the following signs of stomach bleeding:
- you feel faint
- vomit blood
- have bloody or black stools
- have stomach pain that does not get better
- pain gets worse or lasts more than 10 days
- fever gets worse or lasts more than 3 days
- you have difficulty swallowing
- ringing in the ears or loss of hearing occurs
- redness or swelling is present in the painful area
- any new symptoms appear
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Medique Medi-Seltzer Label
Medique®
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Medi-Seltzer
Effervescent Antacid/Pain Reliever
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This Package is for Households without Young Children.
Aches, Fever ● Aspirin (NSAID) 325 mg
Antacid ● Citric Acid 1000 mg Sodium Bicarbonate 1916mg
72 Tablets
(36 x 2)
Tamper Evident Unit Dose Packets
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INGREDIENTS AND APPEARANCE
MEDIQUE MEDI SELTZER
aspirin, citric acid, sodium bicarbonate tablet, effervescentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-135 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 325 mg CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID 1000 mg SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE 1916 mg Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 25mm Flavor Imprint Code L421 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-135-20 18 in 1 BOX 12/30/2008 1 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:47682-135-24 36 in 1 BOX 12/30/2008 2 2 in 1 PACKET; Type 0: Not a Combination Product 3 NDC:47682-135-60 300 in 1 BOX 12/30/2008 3 2 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 part343 12/30/2008 Labeler - Unifirst First Aid Corporation (832947092)