ADVIL MIGRAINE - Haleon US Holdings LLC

Manufacturer: Haleon US Holdings LLC
Effective date: 2026-07-29
Label type: HUMAN OTC DRUG LABEL
Version: 15
Source: daily-update
Hydrated at: 2026-08-01 05:10:11

Label at a glance#

ProductADVIL MIGRAINE

Active ingredientIBUPROFEN

Label structure10 sections

Dosage and administration

do not take more than directed the smallest effective dose should be used adults: take 2 capsules with a glass of water; if symptoms persist or worsen, ask your doctor; do not take more than 2 capsules in 24 hours, unless directed by a doctor under 18 years of age: ask a doctor

Contacts and useful links#

PhoneLabel contact1-800-88-ADVIL

Label contents#

Full prescribing information#

Active ingredient (in each brown oval capsule)

OTC - ACTIVE INGREDIENT SECTION

Solubilized ibuprofen equal to 200 mg ibuprofen (NSAID)*

(present as the free acid and potassium salt)

*nonsteroidal anti-inflammatory drug

Purpose

OTC - PURPOSE SECTION

Pain reliever

Use

INDICATIONS & USAGE SECTION

treats migraine

Warnings

WARNINGS SECTION

Allergy alert:

SPL UNCLASSIFIED SECTION

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.

Stomach bleeding warning:

SPL UNCLASSIFIED SECTION

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:

SPL UNCLASSIFIED SECTION

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.

Medication overuse headache warning:

SPL UNCLASSIFIED SECTION

Headaches may worsen if this product is used for 10 or more days per month.

Do not use

OTC - DO NOT USE SECTION

if you have ever had an allergic reaction to any other pain reliever/fever reducer
right before or after heart surgery

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

you have never had migraines diagnosed by a health professional
you have a headache that is different from your usual migraines
you have the worst headache of your life
you have fever and stiff neck
you have headaches beginning after or caused by head injury, exertion, coughing or bending
you have experienced your first headache after the age of 50
you have daily headaches
you have a migraine so severe as to require bed rest
stomach bleeding warning applies to you
you have problems or serious side effects from taking pain relievers or fever reducers
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

OTC - ASK DOCTOR/PHARMACIST SECTION

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

OTC - WHEN USING SECTION

take with food or milk if stomach upset occurs

Stop use and ask a doctor if

OTC - STOP USE SECTION

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
migraine headache pain is not relieved or gets worse after the first dose
any new symptoms appear

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

do not take more than directed
the smallest effective dose should be used
adults: take 2 capsules with a glass of water; if symptoms persist or worsen, ask your doctor; do not take more than 2 capsules in 24 hours, unless directed by a doctor
under 18 years of age: ask a doctor

Other information

SPL UNCLASSIFIED SECTION

each capsule contains: potassium 20 mg
read all directions and warnings before use. Keep carton.
store at 20-25°C (68-77°F)
avoid excessive heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

D&C yellow no. 10, FD&C green no. 3, FD&C red no. 40, gelatin, pharmaceutical ink, polyethylene glycol, potassium hydroxide, purified water, sorbitol sorbitan solution

Questions or Comments?

OTC - QUESTIONS SECTION

Call toll-free 1-800-88-ADVIL

Additional Information

SPL UNCLASSIFIED SECTION

READ AND KEEP CARTON FOR COMPLETEWARNINGS AND INFORMATION

Do Not Use if seal under bottle cap imprinted with “SEALED for YOUR PROTECTION” is broken or missing.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Advil
MIGRAINE

Solubilized Ibuprofen Capsules, 200 mg
Pain Reliever (NSAID)

Actual Size

20
Liquid Filled
Capsules

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
1e73f975-1ce7-705e-2bcf-788b1b5e24ba	Product name	5	20251124
16cde546-8deb-4df2-a072-dab5566ede95	Product name	1	20231003
f6d1b8d7-3bd1-4248-eddd-b60565c88015	Product name	4	20230808
874f4e63-49d2-5150-5d77-052172814ebd	Product name	6	20230105
557673c2-8256-b351-e863-4ec71a5a64b0	Product name	2	20160714
dbc9a339-6215-4e94-9546-57a3b34902ce	Product name	1	20160517
61c18d4e-b552-5478-8fc0-df38b93e3100	Product name	1	20140508
7b2938c9-7eb7-e312-ae90-f54f4240361e	Product name	1	20140508
997601aa-bb5f-6971-6b90-a21132c12c7b	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0573-0168-20	2024-01-31	C162847	48780-1	1030e365-4d6a-111a-e063-dadaa90a10e2	Drug Facts
0573-0168-20	2024-01-31	C162847	48780-1	1030e365-4d6a-111a-e063-dadaa90a10e2	Drug Facts
0573-0168-30	2024-01-31	C162847	48780-1	1030e365-4d6a-111a-e063-dadaa90a10e2	Drug Facts
0573-0168-30	2024-01-31	C162847	48780-1	1030e365-4d6a-111a-e063-dadaa90a10e2	Drug Facts
0573-0168-40	2024-01-31	C162847	48780-1	1030e365-4d6a-111a-e063-dadaa90a10e2	Drug Facts
0573-0168-40	2024-01-31	C162847	48780-1	1030e365-4d6a-111a-e063-dadaa90a10e2	Drug Facts

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0573-0168-20	EA - Each	0573-0168	feec2afc-1568-4618-bf50-6e30d3943438	1	2012-07-24
0573-0168-30	EA - Each	0573-0168	f0189b18-316b-4562-a067-96974923eda8	1	2012-07-24
0573-0168-40	EA - Each	0573-0168	3d739668-e89f-4a57-9aa7-68e2a5a0dafa	1	2014-06-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
IBUPROFEN	ACTIVE INGREDIENT	WK2XYI10QM	4
IBUPROFEN	ACTIVE MOIETY	WK2XYI10QM	4
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	4
FD&C GREEN NO. 3	INACTIVE INGREDIENT	3P3ONR6O1S	4
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	4
GELATIN	INACTIVE INGREDIENT	2G86QN327L	4
LIGHT MINERAL OIL	INACTIVE INGREDIENT	N6K5787QVP	4
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	4
POTASSIUM HYDROXIDE	INACTIVE INGREDIENT	WZH3C48M4T	4
SORBITAN	INACTIVE INGREDIENT	6O92ICV9RU	4
SORBITOL	INACTIVE INGREDIENT	506T60A25R	4
WATER	INACTIVE INGREDIENT	059QF0KO0R	4

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

ADVIL MIGRAINE
ibuprofen
D&C YELLOW NO. 10
FD&C GREEN NO. 3
FD&C RED NO. 40
GELATIN, UNSPECIFIED
LIGHT MINERAL OIL
POLYETHYLENE GLYCOL, UNSPECIFIED
POTASSIUM HYDROXIDE
WATER
SORBITAN
SORBITOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0573-0168	0573-0168-20, 0573-0168-30, 0573-0168-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
IBUPROFEN	WK2XYI10QM	ACTIB
D&C YELLOW NO. 10	35SW5USQ3G	IACT
FD&C GREEN NO. 3	3P3ONR6O1S	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
GELATIN, UNSPECIFIED	2G86QN327L	IACT
LIGHT MINERAL OIL	N6K5787QVP	IACT
POLYETHYLENE GLYCOL, UNSPECIFIED	3WJQ0SDW1A	IACT
POTASSIUM HYDROXIDE	WZH3C48M4T	IACT
WATER	059QF0KO0R	IACT
SORBITAN	6O92ICV9RU	IACT
SORBITOL	506T60A25R	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
14	2025-10-03	full-release	2026-06-01 01:15:53

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 2 · 120 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
SORBITOL	SORBITOL	506T60A25R	CONCENTRATE / ORAL	600 mg/1ml		Exact identifier — unii+route 72 equally ranked IID candidates
LIGHT MINERAL OIL	LIGHT MINERAL OIL	N6K5787QVP	CAPSULE / ORAL		6 mg	Exact identifier — unii+route 24 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, DELAYED RELEASE / ORAL	0.01 mg		Exact identifier — unii+route 72 equally ranked IID candidates
LIGHT MINERAL OIL	LIGHT MINERAL OIL	N6K5787QVP	CAPSULE / ORAL		6 mg	Exact identifier — unii+route 24 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, COATED / ORAL	12.96 mg		Exact identifier — unii+route 72 equally ranked IID candidates
POTASSIUM HYDROXIDE	POTASSIUM HYDROXIDE	WZH3C48M4T	CAPSULE, LIQUID FILLED / ORAL		154 mg	Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	CONCENTRATE / ORAL	600 mg/1ml		Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, COATED / ORAL	12.96 mg		Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SOLUTION, CONCENTRATE / ORAL	300 mg/1ml		Exact identifier — unii+route 72 equally ranked IID candidates
POTASSIUM HYDROXIDE	POTASSIUM HYDROXIDE	WZH3C48M4T	CAPSULE, LIQUID FILLED / ORAL		154 mg	Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
SORBITAN	SORBITAN	6O92ICV9RU	CAPSULE, LIQUID FILLED / ORAL	NA		Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SUSPENSION / ORAL		45000 mg	Exact identifier — unii+route 72 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE, LIQUID FILLED / ORAL	1.51 mg		Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	CAPSULE / ORAL		1111 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	ELIXIR / ORAL	833.3 mg		Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, FILM COATED / ORAL	5 mg		Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	LIQUID / ORAL		53460 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, EXTENDED RELEASE / ORAL		428 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	POWDER / ORAL		36000 mg	Exact identifier — unii+route 72 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	CAPSULE, LIQUID FILLED / ORAL		1 mg	Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, CHEWABLE / ORAL		3555 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	POWDER / ORAL		36000 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET / ORAL	337.28 mg		Exact identifier — unii+route 72 equally ranked IID candidates
LIGHT MINERAL OIL	LIGHT MINERAL OIL	N6K5787QVP	TABLET, EXTENDED RELEASE / ORAL		1 mg	Exact identifier — unii+route 24 equally ranked IID candidates
LIGHT MINERAL OIL	LIGHT MINERAL OIL	N6K5787QVP	CAPSULE / ORAL		6 mg	Exact identifier — unii+route 24 equally ranked IID candidates
LIGHT MINERAL OIL	LIGHT MINERAL OIL	N6K5787QVP	PASTILLE / ORAL	3.6 mg		Exact identifier — unii+route 24 equally ranked IID candidates
LIGHT MINERAL OIL	LIGHT MINERAL OIL	N6K5787QVP	TABLET, COATED / ORAL	4.8 mg		Exact identifier — unii+route 24 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SUSPENSION / ORAL		45000 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	ELIXIR / ORAL	833.3 mg		Exact identifier — unii+route 72 equally ranked IID candidates
POTASSIUM HYDROXIDE	POTASSIUM HYDROXIDE	WZH3C48M4T	CAPSULE, LIQUID FILLED / ORAL		154 mg	Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
LIGHT MINERAL OIL	LIGHT MINERAL OIL	N6K5787QVP	TABLET / ORAL	7.5 mg		Exact identifier — unii+route 24 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	CAPSULE / ORAL		1111 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	GUM, CHEWING / ORAL		6168 mg	Exact identifier — unii+route 72 equally ranked IID candidates
GELATIN	GELATIN	2G86QN327L	CAPSULE, LIQUID FILLED / ORAL		1042 mg	Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, CHEWABLE / ORAL		3555 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	POWDER / ORAL		36000 mg	Exact identifier — unii+route 72 equally ranked IID candidates
LIGHT MINERAL OIL	LIGHT MINERAL OIL	N6K5787QVP	PASTILLE / ORAL	3.6 mg		Exact identifier — unii+route 24 equally ranked IID candidates
LIGHT MINERAL OIL	LIGHT MINERAL OIL	N6K5787QVP	PASTILLE / ORAL	3.6 mg		Exact identifier — unii+route 24 equally ranked IID candidates
LIGHT MINERAL OIL	LIGHT MINERAL OIL	N6K5787QVP	TABLET, COATED / ORAL	4.8 mg		Exact identifier — unii+route 24 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SOLUTION, CONCENTRATE / ORAL	300 mg/1ml		Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	ELIXIR / ORAL	833.3 mg		Exact identifier — unii+route 72 equally ranked IID candidates
FD&C GREEN NO. 3	FD&C GREEN NO. 3	3P3ONR6O1S	CAPSULE, LIQUID FILLED / ORAL	0.03 mg		Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	GUM, CHEWING / ORAL		6168 mg	Exact identifier — unii+route 72 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE, LIQUID FILLED / ORAL	1.51 mg		Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, FILM COATED / ORAL	5 mg		Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SUSPENSION / ORAL		45000 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, ORALLY DISINTEGRATING / ORAL		7 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SYRUP / ORAL	4370 mg/5ml		Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	POWDER, FOR SUSPENSION / ORAL		12000 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, FILM COATED / ORAL	5 mg		Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, CHEWABLE / ORAL		3555 mg	Exact identifier — unii+route 72 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	CAPSULE, LIQUID FILLED / ORAL		1 mg	Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SOLUTION / ORAL		29268 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, EXTENDED RELEASE / ORAL		428 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	GUM, CHEWING / ORAL		6168 mg	Exact identifier — unii+route 72 equally ranked IID candidates
SORBITAN	SORBITAN	6O92ICV9RU	CAPSULE, LIQUID FILLED / ORAL	NA		Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
FD&C RED NO. 40	FD&C RED NO. 40	WZB9127XOA	CAPSULE, LIQUID FILLED / ORAL		1 mg	Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
FD&C GREEN NO. 3	FD&C GREEN NO. 3	3P3ONR6O1S	CAPSULE, LIQUID FILLED / ORAL	0.03 mg		Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, COATED / ORAL	12.96 mg		Exact identifier — unii+route 72 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	CONCENTRATE / ORAL	600 mg/1ml		Exact identifier — unii+route 72 equally ranked IID candidates

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 · 2 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
N020402-001	ADVIL LIQUI-GELS	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL		RLD, RS	1995-04-20
N020402-002	ADVIL MIGRAINE LIQUI-GELS	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL		RLD, RS	2000-03-16

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.

Product history page 1 of 3 · 86 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	RLD / RS	Approval date	Source SHA-256
2026-09-14 22:38:34	2026-08	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	N020402-001	ADVIL LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	1995-04-20	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020402-002	ADVIL MIGRAINE LIQUI-GELS	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	RLD, RS	2000-03-16	`74a2ff9319b5…`

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ADVIL MIGRAINE	IBUPROFEN	Haleon US Holdings LLC	e4a6219d-4ad4-0119-4cf8-7fc39b4b5979	2026-07-29	Warnings	Exact identifier ndc (package): 0573-0168-20 ndc (package): 0573-0168-30 ndc (package): 0573-0168-40 ndc (product): 0573-0168 ndc11 (package): 00573016840 ndc11 (package): 00573016820 ndc11 (package): 00573016830 spl id: 57c53a9c-1065-d202-e063-6394a90ae1e4 spl set id: e4a6219d-4ad4-0119-4cf8-7fc39b4b5979

Reported adverse events (FAERS/openFDA)#

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