Quick answers
- What is Acetaminophen and pamabrom used for?
- The Drug Facts label of Mantra Menstrual Pain Gel strawberry (Moremed Inc.) lists these uses: For the temporary relief of minor aches and pains and temporary water-weight gain, bloating, swelling, and full feeling associated with the premenstrual and menstrual periods..
- Do I need a prescription for Acetaminophen and pamabrom?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Acetaminophen and pamabrom been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Mantra Menstrual Pain Gel strawberry · Moremed Inc.
Acetaminophen 0.5 g/24 g · Pamabrom 0.025 g/24 g, gel (oral)
Active ingredient (in each 0.85 oz Pouch)
Purpose Acetaminophen 500 mg Pain reliever Pamabrom 25 mg Diuretic
Uses
For the temporary relief of minor aches and pains and temporary water-weight gain, bloating, swelling, and full feeling associated with the premenstrual and menstrual periods.
Warnings
- Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take: more than 4,000 mg of acetaminophen in 24 hours with other drugs containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. 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 nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
- if you are allergic to acetaminophen or pamabrom
- with any other product containing a diuretic
Ask a doctor before use if
you have
- liver disease
- kidney disease
- heart disease
- high blood pressure
- difficulty urinating due to an enlarged prostate gland
Ask a doctor or pharmacist before use if
you are
- taking the blood thinning drug warfarin
Stop use and ask a doctor if
- pain gets worse or lasts more than 10 days
- fever gets worse or lasts more than 3 days
- new symptoms occur
- painful condition persists or gets worse
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. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
Directions
Do not exceed 2 Pouches in 24 hours unless directed by a doctor. Adults and children 12 years and over : take 1 Pouch with every 12 hours as needed. Do not use for more than 10 days, unless directed by a doctor. Children under 12 years : do not use.
Inactive ingredients
Ascorbic Acid, Citric Acid, Glycerin, Manuka Honey, Natural strawberry Flavor, Pectin, Purified Water, Sodium Citrate
— FDA label of Mantra Menstrual Pain Gel strawberry, Moremed Inc., effective August 5, 2026. See the official label on DailyMed →
BackAid Max · Kobayashi Healthcare International, Inc.
Acetaminophen 500 mg · Pamabrom 25 mg, tablet, film coated (oral)
Active ingredient (in each caplet)
Acetaminophen, 500 mg Pamabrom, 25 mg
Purpose
Analgesic (pain reliever) 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 daily 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
symptoms do not improve new symptoms occur pain or fever persists or gets worse
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
Read all package directions and warnings before use. Use only as directed. Adults: Two (2) caplets with a full glass of water every 6 hours while symptoms persist, not to exceed 3 doses (6 caplets) in 24 hours, or as directed by a doctor. Do not exceed recommended dosage. For use by normally healthy adults only. Persons under 18 years of age should use only as directed by a doctor.
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.
— FDA label of BackAid Max, Kobayashi Healthcare International, Inc., effective April 14, 2025. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Acetaminophen 0.5 g/24 g · Pamabrom 0.025 g/24 g · gel (oral) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Mantra Menstrual Pain Gel strawberry | Moremed Inc. | DailyMed |
Acetaminophen 500 mg · Pamabrom 25 mg · tablet, film coated (oral) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| BackAid Max | Kobayashi Healthcare International, Inc. | DailyMed |
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Moremed Inc.1 product
- Kobayashi Healthcare International, Inc.1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.