FDA.reportPublic FDA data

Natural Relief 1222

Manufacturer
RENU LABORATORIES, INC.
Effective date
2022-01-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:15:36

Label at a glance#

ProductNatural Relief 1222
Active ingredientTOXICODENDRON PUBESCENS LEAF, BRYONIA ALBA ROOT
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Bryonia 6x HPUS 1%

Rhus Toxicodendron 6x HPUS 1%

WARNINGS SECTION

For external use only Avoid contact with eyes and open wounds. Stop use and ask a doctor if condition persists for more than 3 days or worsens. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use this product if you are hypersensitive to any of the ingredients.

OTC - STOP USE SECTION

Stop use and ask a doctor if condition persists for more than 3 days or worsens.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PURPOSE SECTION

Muscle aches and stiffness

Joint pain and muscle stiffness

INDICATIONS & USAGE SECTION

Temporry relief of minor pain and stiffness of muscles and joints.

DOSAGE & ADMINISTRATION SECTION

Directions

Apply a small amount of Natural Relief 1222 to affected areas and massage into skin. Use first thing in the morning, before bed, and whenever aches and stiffness flare up.

OTHER SAFETY INFORMATION

Store at 68 ° to 77° F.

STATEMENT OF IDENTITY SECTION

Natural Relief 1222 HOMEOPATHIC JOINT & MUSCLE PAIN RELIEF

INACTIVE INGREDIENT SECTION

Water, Cetearyl Alcohol, Ceteareth-20, Squalene, Propylene Glycol, Prunus Amygdalus Dulcis Oil, Glycine Soja Oil,

Stearic Acid, Tocopherol, Aloe Barbadensis Leaf Juice, SD Alcohol 40-B, Myristyl Myristate, Hydrolyzed Elastin, Hydrolyzed Keratin,

Allium Sativum Bulb Extract, Fragrance, Triethanolamine, Menthol USP, Phenoxyethanol, Benzoic Acid, Dehydroacetic Acid

Natural Relief 1222 Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NATURAL RELIEF 1222 LABEL FOR 32 OZ.

32 oz. NR122232 oz. NR1222

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
baf7f49c-75b6-496b-a00e-8e766a8e4f03Product name120210127
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76348-480-322025-01-30C16284748780-12cef2736-91e1-d83d-e063-dadaa90ab31fNatural Relief 1222

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76348-480-32Natural Relief 1222896 g in 1 BOTTLE, PUMPLOTION8963

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76348-480NATURAL RELIEF 1222 (BRYONIA 6X, RHUS TOXICODENDRON 6X) LOTION [RENU LABORATORIES, INC.]3Legacy NDC, 1 package rows20220118_9dffc462-16e2-bcf1-e053-2995a90a580b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-48076348-480-32

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
STEARIC ACID4ELV7Z65APIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GARLICV1V998DC17IACT
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
MYRISTYL MYRISTATE4042ZC00DYIACT
BRYONIA ALBA ROOTT7J046YI2BACTIB
SQUALANEGW89575KF9IACT
WHITE WAX7G1J5DA97FIACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
HYDROLYZED BOVINE ELASTIN (BASE; 1000 MW)ZR28QKN0WTIACT
MARINE COLLAGEN, SOLUBLE8JC99XGU4WIACT
MENTHOLL7T10EIP3AIACT
ALMOND OIL66YXD4DKO9IACT
SOYBEAN OIL241ATL177AIACT
ALOE VERA LEAFZY81Z83H0XIACT
BENZOIC ACID8SKN0B0MIMIACT
DEHYDROACETIC ACID2KAG279R6RIACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d5c9e83d-60d4-fb9c-e053-2995a90a97319dffc462-16e2-bcf1-e053-2995a90a580b2022-01-17WarningsExact identifier
spl id: d5c9e83d-60d4-fb9c-e053-2995a90a9731
spl set id: 9dffc462-16e2-bcf1-e053-2995a90a580b

Reported adverse events (FAERS/openFDA)#

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