BACKAID MAX- acetaminophen, pamabrom tablet, film coated 
Alva-Amco Pharmacal Companies, Inc.

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BackAid

Active ingredients (in each caplet)

Acetaminophen, 500 mg

Pamabrom, 25 mg

Purpose

Analgesic (pain reliever)

Diuretic

Uses

For the temporary relief of:

Warnings

Liver Warning: This product contains acetaminophen.  Severe liver damage may occur if you take

Allergy Alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

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

Do not use

Ask a doctor before use if you have liver disease.

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.

Stop use and ask a doctor if

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

Keep out of reach of children. In case of overdose, get medical help or contact a poison control center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

Other information

Inactive ingredients Calcium sulfate, croscarmellose sodium, D&C yellow #10 Lake, FD&C yellow #6 Lake, hypromellose, magnesium oxide, magnesium stearate, microcrystalline cellulose, mineral oil, polyethylene glycol, polyvinylpyrrolidone, potassium gluconate, sodium lauryl sulfate, sodium starch glycolate, sorbitol, starch, stearic acid, talc, titanium dioxide.

Questions?  1-800-792-2582.

Package insert

Aspirin Free

Backache Relief

BACKAID Max

1000 mg Strong per 2 Caplet Dose

Maximum Strength 6 Hour Formula

Active ingredients: Each caplet contains: acetaminophen 500 mg (analgesic/pain reliever) and pamabrom 25 mg (diuretic).

Uses: For the temporary relief of: • minor aches, pains and related discomforts due to muscle strain, spasms or overexertion including those affecting the back, legs and joints. • pressure-caused discomforts due to periodic excess water retention.

Warnings

Liver Warning: This product contains acetaminophen. Severe liver damage may occur if you take • more than 6 caplets in 24 hours, which is the maximum dally amount • with other drugs containing acetaminophen • 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.

Do not use • with any other drug containing acetaminophen (prescription or non-prescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. • for more than 10 days for pain unless directed by a doctor • for more than 3 days for fever unless directed by a doctor.

Ask a doctor before use if you have liver disease.

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.

Stop use and ask a doctor if

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

Keep out of reach of children. In case of overdose, get medical help or contact a poison control center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions:

Other information:

Magnesium content: 5 mg/caplet

**CONTENTS SEALED: Each BACKAID MAX golden-­colored, oval shaped caplet bears the identifying mark "ALVA" and is sealed in a clear plastic blister with a paper/foil backing. Do not use if seal appears broken or if product contents do not match product description. • You may report serious side effects to the phone number provided under Questions? below.

Inactive ingredients Calcium sulfate, croscarmellose sodium, D&C yellow #10 Lake, FD&C yellow #6 Lake, hypromellose, magnesium oxide, magnesium stearate, microcrystalline cellulose, mineral oil, polyethylene glycol, polyvinylpyrrolidone, potassium gluconate, sodium lauryl sulfate, sodium starch glycolate, sorbitol, starch, stearic acid, talc and titanium dioxide.

Questions? 1-800-792-2582

BackAidPDP

BACKAID  MAX
acetaminophen, pamabrom tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52389-153
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
PAMABROM (UNII: UA8U0KJM72) (BROMOTHEOPHYLLINE - UNII:FZG87K1MQ6) PAMABROM25 mg
Inactive Ingredients
Ingredient NameStrength
CALCIUM SULFATE DIHYDRATE (UNII: 4846Q921YM)  
STARCH, CORN (UNII: O8232NY3SJ)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MAGNESIUM OXIDE (UNII: 3A3U0GI71G)  
TALC (UNII: 7SEV7J4R1U)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
POTASSIUM GLUCONATE (UNII: 12H3K5QKN9)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
SORBITOL (UNII: 506T60A25R)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
POVIDONE (UNII: FZ989GH94E)  
Product Characteristics
Colororange (Goldenrod) Scoreno score
ShapeOVALSize15mm
FlavorImprint Code ALVA
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52389-153-282 in 1 CARTON03/01/2011
1NDC:52389-153-0114 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:52389-153-141 in 1 CARTON06/01/2011
2NDC:52389-153-0114 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:52389-153-381 in 1 CARTON09/01/2010
3NDC:52389-153-0338 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4NDC:52389-153-461 in 1 CARTON04/29/2016
446 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:52389-153-355 in 1 CARTON06/01/2011
57 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01302/01/1992
Labeler - Alva-Amco Pharmacal Companies, Inc. (042074856)

Revised: 5/2024
Document Id: 180825ee-1910-21f3-e063-6294a90a6f45
Set id: fb9a5647-b7c9-4820-b148-91060e34cb83
Version: 13
Effective Time: 20240509
 
Alva-Amco Pharmacal Companies, Inc.