BACTIMICINA CHILDRENS PAIN AND FEVER - acetaminophen liquid 
DLC Laboratories, Inc.

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.

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BACTIMICINA ® CHILDREN'S PAIN AND FEVER

Drug Facts

Active ingredient (in each 5 mL = 1 teaspoonful)

Acetaminophen 160 mg

Purpose

Pain reliever/fever reducer

Uses

Temporarily:

Warnings

Liver warning

This product contains acetaminophen. Severe liver damage may occur if your child takes

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

Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:

  • skin reddening
  • blisters
  • rash

If a skin reaction occurs, stop use and seek medical help right away.

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 (prescription or nonprescription). 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 recommended dose (see overdose warning)

Stop use and ask a doctor if

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

These could be signs of a serious condition.

Keep out of reach of children.

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

Weight (lb)Age (yr)Dose (mL or tsp) *
*
or as directed by a doctor
Under 24Under 2 yearsAsk a doctor
24-352-3 years5 mL (1 tsp)
36-474-5 years7.5 mL (1½ tsp)
48-596-8 years10 mL (2 tsp)
60-719-10 years12.5 mL (2½ tsp)
72-9511 years15 mL (3 tsp)

Attention: use only enclosed dosage cup specifically designed for use with this product. Do not use any other dosing device.

Other information

Inactive ingredients

citric acid, FD&C red no. 40, flavor, glycerin, high fructose corn syrup, hydroxypropyl methycellulose, purified water, sodium benzoate, sorbitol, xanthan gum

Questions

1-800-858-3889

Manufactured by
DLC Laboratories, Inc.
Paramount, CA 90723 USA

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label

Alcohol Free

Voltee Para

Español

TRUSTED SINCE 1978

New Look

Children's

Bactimicina®

Ages 2-11 Years

Acetaminophen 160 mg/5 mL

Pain & Fever

Pain/Fever Reducer

Oral Suspension

Ibuprofen-Free • Asprin Free

Natural

Cherry Flavor

4 FL OZ (118 mL) Dosing Cup Included Bactimicina-PF

BACTIMICINA CHILDRENS PAIN AND FEVER  
acetaminophen liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1550
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN160 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 (UNII: WZB9127XOA)  
CORN SYRUP (UNII: 9G5L16BK6N)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
WATER (UNII: 059QF0KO0R)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITOL (UNII: 506T60A25R)  
GLYCERIN (UNII: PDC6A3C0OX)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRY (Cherry Flavor) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1550-41 in 1 BOX11/17/2014
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34311/17/2014
Labeler - DLC Laboratories, Inc. (093351930)
Establishment
NameAddressID/FEIBusiness Operations
DLC Laboratories, Inc.093351930manufacture(24286-1550) , label(24286-1550)

Revised: 12/2022
Document Id: ef1d29b1-242a-cffc-e053-2995a90a135c
Set id: bdade270-d813-4178-b594-4951632b6839
Version: 7
Effective Time: 20221205
 
DLC Laboratories, Inc.