Dosage and administration
take only one dose (30 mL) per day (24 hours) only use the dose cup provided only use as directed adults & children 12 yrs & over 30 mL at bedtime children under 12 yrs do not use
Vicks
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Effective date
- 2026-10-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 10
- Source
- daily-update
- Hydrated at
- 2026-10-07 01:01:57
Label at a glance#
ProductVicks PainQuil PM PAIN RELIEVER plus NIGHTTIME SLEEP-AID
Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE, ACETAMINOPHEN
Label structure12 sections
Storage and handling
each 30 mL contains: sodium 89 mg do not exceed 25°C and do not refrigerate.
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active ingredients (in each 30 mL)
Acetaminophen 1000 mg
Diphenhydramine HCl 50 mg
Purpose
Pain reliever
Nighttime sleep-aid
Use
- for the temporary relief of occasional minor aches and pains with accompanying sleeplessness.
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take
- more than 3 doses (30 mL each) in 24 hours, which is the maximum daily amount for this product
- 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
Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
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.
- for children under 12 years of age
- with any other product containing diphenhydramine, even one used on skin
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have
- liver disease
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
- a sodium-restricted diet
OTC - ASK DOCTOR/PHARMACIST SECTION
Ask a doctor or pharmacist before use if you are
- taking the blood thinning drug warfarin
- taking sedatives or tranquilizers
OTC - STOP USE SECTION
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
- redness or swelling is present
- new symptoms occur
- sleeplessness persists continuously for more than 2 weeks.
Insomnia may be a symptom of serious underlying medical illness.
These could be signs of a serious condition.
OTC - WHEN USING SECTION
When using this product
- avoid alcoholic beverages
- drowsiness will occur
- do not drive a motor vehicle or operate machinery
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.
OVERDOSAGE SECTION
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
- take only one dose (30 mL) per day (24 hours)
- only use the dose cup provided
- only use as directed
| adults & children 12 yrs & over | 30 mL at bedtime |
| children under 12 yrs | do not use |
Other information
- each 30 mL contains: sodium 89 mg
- do not exceed 25°C and do not refrigerate.
Inactive ingredients
alcohol, anhydrous citric acid, FD&C Blue No. 1, FD&C Red No. 40, flavor, polysorbate 20, propylene glycol, saccharin sodium, sodium benzoate, sodium chloride, sodium citrate, sorbitol, sucralose, water, xanthan gum
Questions?
1-877-881-5813
SPL UNCLASSIFIED SECTION
TAMPER EVIDENT: DO NOT USE IF PRINTED SHRINKBAND IS BROKEN OR MISSING.
SPL UNCLASSIFIED SECTION
DIST. BY: PROCTER & GAMBLE,
CINCINNATI, OH 45202
PRINCIPAL DISPLAY PANEL - 354 ml bottle
VICKS ®
PainQuil™ PM
PAIN RELIEVER + NIGHTTIME SLEEP-AID
Acetaminophen
Diphenhydramine HCl
STARTS WORKING FAST
FOR RELIEF OF:
ACHES | PAINS
HEADACHE | SORE THROAT
+ OCCASSIONAL SLEEPLESSNESS
MIDNIGHT CHERRY FLAVORED
Alcohol 10%
12 FL OZ (354 ml)
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0030772138830 | GTIN-13: 0030772138830 EAN-13: 0030772138830 GTIN-12: 030772138830 UPC-A: 030772138830 GTIN storage (14 digits): 00030772138830 | 834.jpg |
| Data code | Data Matrix | 21009133 | 834.jpg | |
| Data code | Data Matrix | 21463007 | 834.jpg |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 0e2e0f88-b076-afe1-4bdd-32bca4375bec | Product name | 3 | 20250127 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 3e48c9c4-918d-5d23-2f0b-d2398b06be54 | Product name | 1 | 20140508 |
| 865c72dd-0d94-daac-f728-ddd4ded2a79e | Product name | 1 | 20140508 |
Products#
Every source-derived product name is available through these pages.
- Vicks PainQuil PM PAIN RELIEVER plus NIGHTTIME SLEEP-AID
- Acetaminophen, Diphenhydramine HCl
- DIPHENHYDRAMINE HYDROCHLORIDE
- DIPHENHYDRAMINE
- ACETAMINOPHEN
- PROPYLENE GLYCOL
- ALCOHOL
- CITRIC ACID MONOHYDRATE
- POLYSORBATE 20
- SACCHARIN SODIUM
- WATER
- FD&C RED NO. 40
- SODIUM BENZOATE
- SODIUM CHLORIDE
- SODIUM CITRATE
- SORBITOL
- SUCRALOSE
- XANTHAN GUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69423-834 | 69423-834-12, 69423-834-24 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | TC2D6JAD40 | ACTIB |
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| POLYSORBATE 20 | 7T1F30V5YH | IACT |
| SACCHARIN SODIUM | SB8ZUX40TY | IACT |
| WATER | 059QF0KO0R | IACT |
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| SODIUM CITRATE | 1Q73Q2JULR | IACT |
| SORBITOL | 506T60A25R | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 9 | 2026-07-20 | daily-update | 2026-07-25 05:10:34 |
| 8 | 2025-12-01 | full-release | 2026-06-01 01:18:52 |
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 |
|---|---|---|---|---|---|---|
| 570df25f-4e31-1f79-e063-6294a90a7f13 | 65803fcd-3f5b-4c9d-85a1-2bf03ed6f68d | 2026-07-20 | Warnings | 65803fcd-3f5b-4c9d-85a1-2bf03ed6f68d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.