Dr Simi Pain Reliever PM

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Dr Simi Pain Reliever PM
Generic name
ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE
Manufacturer
Farmacias De Similares TX LLC
Product type
HUMAN OTC DRUG
SPL set ID
3c19ad99-6e0f-3116-e063-6394a90a914c
SPL ID
3c19ad99-6e10-3116-e063-6394a90a914c
Version
1
Effective date
2025-08-11
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:06:00
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take. More than 2 caplets in 24 hours, which is the maximum daily amount for this product. With other drugs containing acetaminophen. 3 or more alcoholicdrinks everyday 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.

Reported adverse events (FAERS/openFDA)#

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