FAST ACTING PEDIA CRAE- acetaminophen suspension

Fast Acting by

Drug Labeling and Warnings

Fast Acting by is a Otc medication manufactured, distributed, or labeled by Randob Labs., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each 5 mL)

Acetaminophen 160 mg

Purpose

Pain reliever/fever reducer

Uses

temporarily:

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

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

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222) 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.
• ▪ do not give more than directed (seeoverdose warning)
• ▪ shake well before using
• ▪ mL = milliliter
• ▪ find right dose on chart. If possible, use weight to dose; otherwise, use age.
• ▪ remove the child protective cap and squeeze your child’s dose into the dosing cup
• ▪ do not give more than 5 times in 24 hours

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

**or as directed by a doctor

Attention: use only enclosed dosing cupl specifically designed for use with this product.

Do not use any other dosing device.

Other information

• ▪ very low sodium
• ▪ store at room temperature

Inactive ingredients

anhydrous citric acid, carboxymethylcellulose sodium, flavors, glycerin, microcrystalline cellulose, sodium benzoate, purified water, sodium citrate dihydrate, sorbitol liquid, sucralose, xanthan gum

Questions?

1-866-467-2748

PRINCIPAL DISPLAY PANEL

NDC: 52412-912-01

Fast Acting

Pedia Care®

100% dedicated to kids™

Infants

ACETAMINOPHEN

Pain Reliever / Fever Reducer

Acetaminophen (160mg per 5 mL)

Oral Suspension

• No Added Alcohol
• Ibuprofen Free
• Aspirin Free
• No Parabens

Natural Grape Flavor

(Use only Enclosed Syringe)

1 FL OZ (30 mL)
160 mg per 5 mL

TAMPER EVIDENT: DO NOT USE IF PRINTED SEAL OVER CAP IS BROKEN OR MISSING

IMPORTANT: Keep this carton for future reference on full labeling.

Package Label of 1 FLOZ (30 mL)

Package Label of 4 FLOZ (118 mL)

INGREDIENTS AND APPEARANCE

FAST ACTING  PEDIA CRAE
acetaminophen suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52412-912
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
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
GLYCERIN (UNII: PDC6A3C0OX)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
SORBITOL SOLUTION (UNII: 8KW3E207O2)
SUCRALOSE (UNII: 96K6UQ3ZD4)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor	GRAPE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52412-912-01	1 in 1 CARTON	05/26/2023
1		30 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package
2	NDC: 52412-912-04	1 in 1 CARTON	05/26/2023
2		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 not final	part343	05/26/2023

Labeler - Randob Labs., Ltd. (061995007)