AY BENDITO HEMP

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
AY BENDITO HEMP
Generic name
MENTHOL, CAMPHOR
Manufacturer
AY BENDITO INTERNATIONAL, INC
Product type
HUMAN OTC DRUG
SPL set ID
457c9bd6-2e72-03e5-e063-6394a90a558c
SPL ID
457cab9c-93a3-c814-e063-6294a90aea61
Version
1
Effective date
2025-12-08
Source export date
2026-11-06
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:26:45
Harmonized routes table
Harmonized routes
TOPICAL

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

For external use only. Do not apply to wounds or damaged skin, with a heating pad or on a child under 12 years of age. Flammable Keep away from fire or flame. Use only as directed. Do not bandage tightly. Avoid contact with eyes and mucous membranes. If you experience an allergic reaction, discontinue use, and consult a doctor. Do not expose the area treated with product to heat or direct sunlight. Stop use and ask a doctor if Condition worsens. Redness is present. Irritation develops. Symptoms persist for more than 7 days or clear up occur again within a few days. You experience signs of injury, such as pain, swelling or blistering where the product was applied. If pregnant or breast – feeding Ask a health professional before use. Keep out of reach of children If swallowed, get medical help, or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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