AMP RELIEF Pain Relief Cream

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: AMP RELIEF Pain Relief Cream
Generic name: MENTHOL
Manufacturer: COASTAL FORMULAS LLC
Product type: HUMAN OTC DRUG
SPL set ID: 84ea496e-ab54-4882-93ef-600f8eb33cb4
SPL ID: 09e32c60-2b72-0226-e063-6294a90a6a2f
Version: 2
Effective date: 2023-11-11
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:03:22

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		AMP RELIEF Pain Relief Cream	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		COASTAL FORMULAS LLC	openfda.manufacturer_name
ndc	package	82560-283-00	openfda.package_ndc
ndc	product	82560-283	openfda.product_ndc
ndc11	package	82560028300	derived:openfda.package_ndc
rxcui		727161	openfda.rxcui
spl id		09e32c60-2b72-0226-e063-6294a90a6a2f	id
spl set id		84ea496e-ab54-4882-93ef-600f8eb33cb4	set_id
unii		L7T10EIP3A	openfda.unii

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

Warnings: For external use only. Do not use on damaged or broken skin When using this product Avoid contact with the eyes. Do not bandage tightly. Stop use and ask a doctor if rash or irritation develops and lasts condition worsens sysmptoms persist for more than 7 days clears up and occurs again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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