FEVERALL ADULTS- acetaminophen suppository

Feverall by

Drug Labeling and Warnings

Feverall by is a Otc medication manufactured, distributed, or labeled by Taro Pharmaceuticals U.S.A. Inc., G&W NC Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredient (in each rectal suppository)

Acetaminophen, USP 650 mg

Purposes

Pain reliever/fever reducer

Uses

temporarily

• reduces fever
• relieves minor aches, pains, and headache

Warnings

Liver warning

This product contains acetaminophen. Severe liver damage may occur if

• an adult or child 12 years and older takes more than 6 doses in 24 hours, which is the maximum daily amount
• taken with other drugs containing acetaminophen
• an adult takes 3 or more alcoholic drinks every day while using this product

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.

For rectal use only.

Do not use

• in children under 12 years.
• if you are allergic to acetaminophen.
• with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

Ask a doctor before use if

• you have liver disease.
• you are taking the blood thinning drug warfarin.

Stop use and ask a doctor if

• fever lasts more than 3 days (72 hours), or recurs.
• pain gets worse or lasts more than 10 days.
• new symptoms occur.
• redness or swelling is present in the painful area.

These may be signs of a serious condition.

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

Keep out of reach of children. If swallowed or in case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical in case of overdose for adults and for children even if you do not notice any signs or symptoms.

Directions

• do not use more than directed
• remove wrapper
• carefully insert suppository well up into the rectum
• adults and children 12 years and older:
  • 1 suppository every 4 to 6 hours while symptoms last
  • do not exceed 6 suppositories in any 24-hour period
• children under 12 years: ask a doctor

Other information

• store at 2°-27°C (35°-80°F)
• do not use if imprinted suppository wrapper is opened or damaged

Inactive ingredients

glycerol monostearate, hydrogenated vegetable oil, polyoxyethylene stearate, polysorbate 80

Questions?

call 1-866-923-4914

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Distributed by:
Taro Pharmaceuticals U.S.A., Inc.
Hawthorne, NY 10532

PRINCIPAL DISPLAY PANEL - 50 Suppository Carton

ADULTS'
ages 12 years & older

FeverAll®
ACETAMINOPHEN SUPPOSITORIES

Pain Reliever/Fever Reducer

NOT FOR RETAIL SALE
NDC: 51672-2117-4

RECTAL
SUPPOSITORY*

*actual size

Doctor Recommended

50
Rectal
Suppositories

650
mg
each

INGREDIENTS AND APPEARANCE

FEVERALL   ADULTS
acetaminophen suppository

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51672-2117
Route of Administration	RECTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D)	Acetaminophen	650 mg

Inactive Ingredients
Ingredient Name	Strength
glyceryl monostearate (UNII: 230OU9XXE4)
hydrogenated palm kernel oil (UNII: FM8D1RE2VP)
PEG-100 stearate (UNII: YD01N1999R)
polysorbate 80 (UNII: 6OZP39ZG8H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51672-2117-4	50 in 1 CARTON	12/12/2013
1	NDC: 51672-2117-0	1 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NDA	NDA018337	12/12/2013

Labeler - Taro Pharmaceuticals U.S.A. Inc. (145186370)

Establishment
Name	Address	ID/FEI	Business Operations
G&W NC Laboratories, Inc.		079419931	MANUFACTURE(51672-2117)