TEMP X- acetaminophen suspension

Temp X by

Drug Labeling and Warnings

Temp X by is a Otc medication manufactured, distributed, or labeled by OPMX Chula Vista, Bajaj Medical, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(in each 5 mL) Purpose

Acetaminophen 160 mg............. Pain reliever/fever reducer

PURPOSE

Pain Reliever & Fever Reducer

Uses

temporarily:

• reduces fever
• relieves minor aches and pains due to:
• sore throat
• the common cold
• flu
• headache
• toothache

Warnings

Liver warning: This product contains acetaminophen.

Severe liver damage may occur if your child takes takes

• more than 5 doses in 24 hours. which is the maximum daily amount.
• with other drugs containing acetaminophen.

Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Do not use

• with any other drug containing acetaminophen (prescnption or non-prescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
• if your child is allergic to acetaminophen or any of the inactive ingredients in this product.

Ask a doctor before use if your child has liver disease.

Ask a doctor or pharmacist before use if your child is taking the blood thinning drug warfarin.

When using this product do not exceed recommened dose (see overdose warning)

STOP USE

Stop use and ask a doctor if

• new sympthoms occur
• redness or swelling is present
• pain gets worse or lasts more than 5 days
• fever gets worse or lasts more than 3 days

These could be signs of a serious condition

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

OVERDOSAGE

Overdose warning: Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

• this product does not contain directions or complete warnings for adult use. Shake well before using
• mL= millilitar
• find right dose on chart below, if possible, use weight to dose; otherwise, use age
• repeat dose every 4 hours while symptoms last
• only use enclosed measuring syringe
• do not give more than 5 times in 24 hours
• do not give more than 5 days unless directed by a doctor

Weight (lb,)	Age (yrs.)	Dose (mL)*
Under 24	Under 2	Ask a doctor
24-35	2-3	5 mL
36-47	4-5	7.5 mL
48-59	6-8	10 mL
60-71	9-10	12.5 mL
72-95	11	15 mL

*always check with your doctor before administering medicine to your infant/child

Other information

• Each teaspoon (5 mL) contains: sodium 3 mg
• Store between 15°-30°C (59°-86°F)
• Protect from freezing. Protect from light

Inactive ingredients

acesulfame potassium, citric acid, FD&C red no. 40, flavor, glycerine, high fructose corn syrup, microcrystalline cellulose and carboxymethylcellulose sodium, polysorbate, propylene glycol, prosweet N&AK, purified water, sodium benzoate, sucralose, sorbitol, xanthan gum.

Questions or comments?

Call toll free 619-600-5632

Monday through Fnday 9AM - 5PM EST

PRINCIPAL DISPLAY PANEL

NDC: 69729-047-04 Temp X

INGREDIENTS AND APPEARANCE

TEMP X 
acetaminophen suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69729-047
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	160 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SORBITOL (UNII: 506T60A25R)
XANTHAN GUM (UNII: TTV12P4NEE)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69729-047-04	1 in 1 CARTON	06/02/2023
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	06/02/2023

Labeler - OPMX Chula Vista (029918743)

Establishment
Name	Address	ID/FEI	Business Operations
Seaway Pharma		117218785	manufacture(69729-047)