Green Guard Maximum Strength Non-Aspirin
- Manufacturer
- Unifirst First Aid Corporation | Prestige Packaging | Medique Products
- Effective date
- 2025-09-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- full-release
- Hydrated at
- 2026-06-01 01:13:08
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active ingredient (in each tablet)
Acetaminophen 500 mg
OTC - PURPOSE SECTION
Purpose
Pain reliever/fever reducer
INDICATIONS & USAGE SECTION
Uses
temporarily relieves minor aches and pains due to:
- headache
- muscular aches
- minor pain of arthritis
- backache
- the common cold
- toothache
- premenstrual and menstrual cramps
temporarily reduces fever
WARNINGS SECTION
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:
- more than 4,000 mg 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.
OTC - DO NOT USE SECTION
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 any of the inactive ingredients in this product
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have
- liver disease
OTC - ASK DOCTOR/PHARMACIST SECTION
Ask a doctor or pharmacist before use if
- you are taking the blood thinning drug warfarin
OTC - STOP USE SECTION
Stop use and ask a doctor if
- pain gets worse or lasts more than for more than 10 days
- fever gets worse or lasts more than 3 days
- new symptoms occur
- redness or swelling is present
These could be signs of a serious condition.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
Overdose Warning:
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
DOSAGE & ADMINISTRATION SECTION
Directions
do not use more than directed (see overdose warning)
Adults and children (12 years and over)
- take 2 tablets every 6 hours while symptoms last.
- do not take more than 6 tablets in 24 hours, unless directed by a doctor
- do not use for more than 10 days unless directed by a doctor
Children under 12 years: Ask a doctor
OTHER SAFETY INFORMATION
Other information
- store at room temperature 59º-86ºF (15º-30ºC)
- tamper-evident sealed packets
- do not use any opened or torn packets
INACTIVE INGREDIENT SECTION
Inactive ingredients
corn starch*, hypromellose*, polyethylene glycol*, povidone (K-30)*, pregelatinized starch*, purified water*, sodium starch glycolate, stearic acid, titanium dioxide*
may contain*
OTC - QUESTIONS SECTION
Questions or comments? 1-800-869-6970
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Maximum Strength Non-Aspirin relief
Acetaminophen 500 mg/Acetaminofeno 500 mg
Pain Reliever/Fever Reducer
Alivia el Dolor/Reduce la Fiebre
Compare Active Ingredient To Extra Strength Tylenol®
Green Guard®
Pull Out
Tire Para Abrir
Tylenol® is a Registered Trademark of McNeil Consumer Products
50 Packets of 2 Tablets
100 Tablets
Order #2224
Distributed by Green Guard® St Louis. MO 63045
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Maximum Strength Non-Aspirin relief
Acetaminophen 500 mg/Acetaminofeno 500 mg
Pain Reliever/Fever Reducer
Alivia el Dolor/Reduce la Fiebre
Compare Active Ingredient To Extra Strength Tylenol®
Green Guard®
Pull Out
Tire Para Abrir
Tylenol® is a Registered Trademark of McNeil Consumer Products
50 Packets of 2 Tablets
100 Tablets
Order #2224
Distributed by Green Guard® St Louis. MO 63045
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 47682-170-33 | Green Guard Maximum Strength Non-Aspirin | 50 in 1 BOX | TABLET | 50 | 5 | |
| 47682-170-48 | Green Guard Maximum Strength Non-Aspirin | 125 in 1 BOX | TABLET | 125 | 5 | |
| 47682-170-99 | Green Guard Maximum Strength Non-Aspirin | 2 in 1 PACKET | TABLET | 2 | 5 | |
| 47682-619-33 | Green Guard Maximum Strength Non-Aspirin | 50 in 1 CARTON | TABLET, FILM COATED | 50 | 5 | |
| 47682-619-48 | Green Guard Maximum Strength Non-Aspirin | 125 in 1 CARTON | TABLET, FILM COATED | 125 | 5 | |
| 47682-619-99 | Green Guard Maximum Strength Non-Aspirin | 2 in 1 PACKET | TABLET, FILM COATED | 2 | 5 |
Products#
Every source-derived product name is available through these pages.
- Green Guard Maximum Strength Non-Aspirin
- Acetaminophen
- STARCH, CORN
- POVIDONE
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- STEARIC ACID
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POVIDONE K30
- HYPROMELLOSE, UNSPECIFIED
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 47682-170 | 47682-170-99, 47682-170-33, 47682-170-48 |
| 47682-619 | 47682-619-99, 47682-619-33, 47682-619-48 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| Green Guard Maximum Strength Non-Aspirin | ACETAMINOPHEN | Unifirst First Aid Corporation | f77c9554-d1c2-1682-e053-6294a90ac572 | 2025-09-08 | Warnings | 47682-170-33 47682-170-99 47682-170-48 47682-619-33 47682-619-99 47682-619-48 47682-170 47682-619 47682017033 47682017099 47682061933 47682061999 47682061948 47682017048 3e4cbfac-83b3-bda3-e063-6294a90a9abd f77c9554-d1c2-1682-e053-6294a90ac572 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

