Indications and uses
For the temporary relief of minor aches and pains associated with • headache • common cold • muscular aches • toothache • minor arthritis pain • menstrual cramps For the reduction of fever.
MEDI-FIRST Non-Aspirin
- Manufacturer
- Proficient Rx LP
- Effective date
- 2024-02-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 00:08:41
Label at a glance#
ProductMEDI-FIRST Non-Aspirin
Active ingredientACETAMINOPHEN
Label structure8 sections
Dosage and administration
• do not use more than directed Take 2 tablets every 4 to 6 hours as needed. Do not take more than 12 tablets in 24 hours. Do not give to children under 12 years of age. • store at room temperature 59°-86°F (15°-30°C) • tamper-evident sealed packets • do not use any opened or torn packets
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient (in each tablet)
Acetaminophen 325 mg
Purpose
Pain reliever/fever reducer
Uses
For the temporary relief of minor aches and pains associated with
- headache
- common cold
- muscular aches
- toothache
- minor arthritis pain
- menstrual cramps
For the reduction of fever.
Warnings
SPL UNCLASSIFIED SECTION
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:
- more than 12 tablets 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 nonprescription). 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 using and ask a doctor if
- symptoms do not improve
- new symptoms occur
- pain or fever persists or gets worse
- redness or swelling is present
If pregnant or breast-feeding,
ask a health professional before use.
Keep out of reach of children.
In case of accidental 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
- do not use more than directed
Adults and children: (12 years and older)
Take 2 tablets every 4 to 6 hours as needed. Do not take more than 12 tablets in 24 hours.
Children under 12 years:
Do not give to children under 12 years of age.
Other information
- store at room temperature 59°-86°F (15°-30°C)
- tamper-evident sealed packets
- do not use any opened or torn packets
Inactive ingredients
corn starch, hypromellose, maltodextrin*, microcrystalline cellulose*, polyethylene glycol, povidone*, pregelatinized starch*, sodium starch glycolate*, stearic acid, titanium dioxide*
* may contain
Questions or comments?
1-800-634-7680
Medi-First Non-Aspirin 325 mg Label
4 Tablets
71205-306-04
Medi-First ®
Non-Aspirin
Aches, Fever ● Acetaminophen 500mg
Dolores, Fiebre ● Acetaminofeno 500mg
Aspirin-Free Pain Relief
Pull to Open
Tire Para Abrir
Compare active ingredients to:
Compare el ingrediente activo con:
Extra Strength Tylenol®
Registered Trademark of McNeil Consumer Products
Marca Registrada de McNeil Consumer Products
Tamper Evident Unit Dose Packets
Empaquetado con Sellado
Evidente en Dosis Unitarias
Relabeled by:
Proficient Rx LP
Thousand Oaks, CA 91320
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71205-306-04 | MEDI-FIRST Non-Aspirin | 4 in 1 PACKET | TABLET, COATED | 4 | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 47682-803-13 | EA - Each | 47682-803 | 69053d1e-b259-4b5f-acef-863753677b30 | 1 | 2012-07-24 |
| 47682-803-33 | EA - Each | 47682-803 | 6ce7f5f9-a8ad-46aa-99c7-b186bf154ad7 | 1 | 2012-07-24 |
| 47682-803-48 | EA - Each | 47682-803 | a94b0390-13d0-4b1c-a159-24abff09e0bb | 1 | 2012-07-24 |
| 47682-803-99 | EA - Each | 47682-803 | a3e93432-20eb-4fdf-a9cf-ff2be36d91c4 | 1 | 2022-06-06 |
Products#
Every source-derived product name is available through these pages.
- MEDI-FIRST Non-Aspirin
- Acetaminophen
- HYPROMELLOSE, UNSPECIFIED
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POVIDONE, UNSPECIFIED
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- STARCH, CORN
- STEARIC ACID
- TITANIUM DIOXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71205-306 | 71205-306-04 |
| 47682-803 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
| POVIDONE, UNSPECIFIED | FZ989GH94E | IACT |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | 5856J3G2A2 | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Medique APAP | ACETAMINOPHEN | Unifirst First Aid Corporation | 04805d9c-d959-4870-a185-48b58a880880 | 2025-09-08 | Warnings | 47682-803 |
| MEDI-FIRST Non-Aspirin | ACETAMINOPHEN | Proficient Rx LP | 4c84948d-3a95-4c53-8529-7e7b9d8bb6df | 2024-02-01 | Warnings | 71205-306-04 71205-306 71205030604 4eb6a025-a57e-46fa-938b-25c93d4627aa 4c84948d-3a95-4c53-8529-7e7b9d8bb6df |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.