Home FDA labels 0ee19610-a0da-4a88-b64c-8759953d7cda Muscle Ice 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 Muscle Ice
Generic name PHYTOLACCA DECANDRA, BELLIS PERENNIS, LEDUM PALUSTRE, RUTA GRAVEOLENS, SYMPHYTUM OFFICINALE, MAGNESIA PHOSPHORICA, SILICEA, MENTHOL (CRYSTALS)
Manufacturer Peaceful Mountain, Inc.
Product type HUMAN OTC DRUG
SPL set ID 03b6e2a9-f335-4ae2-9011-80bd019afb72
SPL ID 0ee19610-a0da-4a88-b64c-8759953d7cda
Version 5
Effective date 2026-07-30
Source export date 2026-09-28
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:18:23 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 · 15 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Muscle Ice openfda.brand_name generic name PHYTOLACCA DECANDRA, BELLIS PERENNIS, LEDUM PALUSTRE, RUTA GRAVEOLENS, SYMPHYTUM OFFICINALE, MAGNESIA PHOSPHORICA, SILICEA, MENTHOL (CRYSTALS) openfda.generic_name manufacturer name Peaceful Mountain, Inc. openfda.manufacturer_name ndc package 43846-0073-1 openfda.package_ndc ndc product 43846-0073 openfda.product_ndc ndc11 package 43846007301 derived:openfda.package_ndc spl id 0ee19610-a0da-4a88-b64c-8759953d7cda id spl set id 03b6e2a9-f335-4ae2-9011-80bd019afb72 set_id unii 877L01IZ0P openfda.unii unii 11E6VI8VEG openfda.unii unii 2HU33I03UY openfda.unii unii N94C2U587S openfda.unii unii HF539G9L3Q openfda.unii unii ETJ7Z6XBU4 openfda.unii unii M9VVZ08EKQ 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. Avoid contact with eyes. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. Do not apply to wounds or damaged skin, or mucous membranes. Do not bandage tightly. 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. Do not use if saftey seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.