Active Ingredients

Manufacturer
Kai Squared | Allegiant Health
Effective date
2026-06-01
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
daily-update
Hydrated at
2026-06-04 05:10:14

Label at a glance#

ProductPeriod Pills by Biikay
Active ingredientACETAMINOPHEN, IBUPROFEN
Label structure12 sections

Indications and uses

Temporarily relieves minor aches and pains due to: headache, toothache, backache, menstrual cramps, muscular aches, minor pain of arthritis

Dosage and administration

Do not take more than directed Adults and children 12 years and over: take 2 caplets every 8 hours while symptoms persist; Children under 12 years ask a doctor Do not take more than 6 caplets in 24 hours, unless directed by a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients (in each caplet) Purpose

Acetaminophen 250 mg Pain reliever

Ibuprofen 125 mg (NSAID**) Pain reliever

**nonsteroidal anti-inflammatory drug

PURPOSE

OTC - PURPOSE SECTION

Pain Reliever

USES(S)

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains due to: headache, toothache, backache, menstrual cramps, muscular aches, minor pain of arthritis

WARNINGS SECTION

Acetaminophen liver damage warning: This product contains acetaminophen. Severe liver damage may occur if you take: with other drugs containing acetaminophen, more than 6 caplets in 24 hours, which is the maximum daily amount for this product, 3 or more alcoholic drinks every day while using this product.


Acetaminophen allergy alert: may cause severe skin reactions. Symptoms include, skin reddening, blisters, rash.
If skin reactions occurs, stop use and seek medical help right away.


NSAID allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin.

Symptoms may include: hives, facial swelling, asthma (wheezing), shock, skin reddening, rash, blisters
If an allergic reaction occurs, stop use and seek medical help right away.


NSAID stomach bleeding warnings: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you: are age 60 or older, have had stomach ulcers or bleeding problems, take a blood thinning (anticoagulant) or steroid drug, take other drugs containing prescription or nonprescription NSAIDs [aspirin, ibuprofen, naproxen, or others], have 3 or more alcoholic drinks every day while using this product, take more or for a longer time than directed.


Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

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 have ever had an allergic reaction to acetaminophen or any other pain reliever, right before or after heart surgery.

Ask a doctor before use if:

You have liver disease, stomach bleeding warning applies to you, you have problems or serious side effects from taking pain relievers, you have a history of stomach problems such as heartburn, you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke, you are taking a diuretic.

Ask a doctor or pharmacist before use if you are:

Under a doctor’s care for any serious condition, taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin, taking any other drug.

When using this product, take with food or milk if stomach upset occurs.

Stop use and ask a doctor if, you experience any of the following signs of stomach bleeding:

feel faint, vomit blood, have bloody or black stools, have stomach pain that does not get better, you have symptoms of heart problems or stroke: chest pain, trouble breathing, weakness in one part or side of body, slurred speech, leg swelling, pain gets worse or lasts more than 10 days, redness or swelling is present in the painful area, any new symptoms appear.

If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use ibuprofen at 20 weeks or later in pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) 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

DOSAGE & ADMINISTRATION SECTION

  • Do not take more than directed

Adults and children 12 years and over: take 2 caplets every 8 hours while symptoms persist;

Children under 12 years ask a doctor

  • Do not take more than 6 caplets in 24 hours, unless directed by a doctor

Other Information

OTHER SAFETY INFORMATION

  • Read all warnings and directions before use.
  • Store at 20 to 25°C (68 to 77°F).
  • Avoid excessive heat above 40°C (104°F).
  • Do not use if imprinted safety seal under cap is broken or missing.

INACTIVE INGREDIENT SECTION

Inactive ingredients:

carnauba wax, colloidal silicon dioxide, croscarmellose sodium, crospovidone, ferric oxide red, ferric oxide yellow, hypromellose, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, povidone, pregelatinized starch, sodium lauryl sulfate, stearic acid and titanium dioxide.

Questions/Comments

OTC - QUESTIONS SECTION

Call 1-800-997-5561, Monday through Friday, 9AM-5PM EST.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use ibuprofen at 20 weeks or later in pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

RECENT MAJOR CHANGES SECTION

Relabeling of sections to conform to SPL requirements

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelPeriod Pills by Biikay

Pain Reliever

Carton ImageCarton Image

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
IBUPROFEN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20191108

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130385576101369GTIN-13: 0385576101369
EAN-13: 0385576101369
GTIN-12: 385576101369
UPC-A: 385576101369
GTIN storage (14 digits): 00385576101369
Label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85576-10185576-101-36

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62026-03-22full-release2026-06-01 01:51:03
52026-01-02monthly-update2026-06-03 17:51:16
42025-12-24monthly-update2026-06-03 17:47:03

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A216592-001ACETAMINOPHEN AND IBUPROFENACETAMINOPHEN; IBUPROFEN250MG;125MGTABLET / ORAL2023-07-13

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-1384e616aacf4f…
2026-08-18 06:07:402026-07A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-13caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-13011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-1331067a03dcf5…
2025-08-23 18:47 UTC2025-08A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-136a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-13fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-13b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-1303ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-132680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-135bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-13d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-13d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-1379d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-13301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-131e350fbaab3a…
2024-05-31 18:47 UTC2024-05A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-138072bd15b7f6…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-136a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-131c564ffb4f44…
2023-12-20 04:57 UTC2023-12A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-13ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-13a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-139b2671bbb829…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A216592-001ACETAMINOPHEN AND IBUPROFEN250MG;125MGTABLET / ORAL2023-07-13a50c72e98297…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Period Pills by BiikayACETAMINOPHEN, IBUPROFENKai Squared40d2ae73-82cf-3fa1-e063-6394a90a9ea22026-06-01WarningsExact identifier
ndc (package): 85576-101-36
ndc (product): 85576-101
ndc11 (package): 85576010136
spl id: 533260ee-9c48-fe57-e063-6394a90a9130
spl set id: 40d2ae73-82cf-3fa1-e063-6394a90a9ea2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.