Backache Relief

Manufacturer
Hyland's Inc.
Effective date
2023-05-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:21:09

Label at a glance#

ProductBackache Relief
Active ingredientARNICA MONTANA, BELLIS PERENNIS, ACONITUM NAPELLUS, BRYONIA ALBA ROOT, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF
Label structure10 sections

Indications and uses

■ Temporarily relieves backache pain

Dosage and administration

■ Use as directed. Adults and children 12 years and over At onset of symptoms, dissolve 2 tablets under tongue every 15 minutes up to 4 doses. If symptoms persist, 2 tablets every 4 hours until relieved. Children under 12 years of age Ask a doctor before use.

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Backache Relief

Drug Facts

SPL UNCLASSIFIED SECTION

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Purpose

Aconitum Napellus 6X HPUS

backache pain

Arnica Montana 6X HPUS

backache pain

Bellis Perennis 6X HPUS

backache pain

Bryonia Alba 6X HPUS

backache pain

Magnesia Phosphorica 6X HPUS

backache pain

Rhus Toxicodendron 6X HPUS

backache pain

"HPUS" indicates that the active ingredients are in the official Homeopathic

Pharmacopoeia of the United States.

Uses

INDICATIONS & USAGE SECTION

■ Temporarily relieves backache pain

Warnings

WARNINGS SECTION

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ pain gets worse or lasts more than 7 days.
■ new symptoms occur.
■ redness or swelling is present

If pregnant or breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

■ Use as directed.

Adults and children
12 years and over

At onset of symptoms, dissolve 2 tablets under tongue every

15 minutes up to 4 doses. If symptoms persist, 2 tablets every

4 hours until relieved.

Children under
12 years of age
Ask a doctor before use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acacia Gum, Lactose.

Dosage and Administration

RECENT MAJOR CHANGES SECTION

(Directions)

■ Use as directed

Adults and children

12 years and over
At onset of symptoms, dissolve 2 tablets under tongue every

15 minutes up to 4 doses. If symptoms persist, 2 tablets every

4 hours until relieved.
Children under

12 years of age
Ask a doctor before use.

Indications and Usage

RECENT MAJOR CHANGES SECTION

Uses

■ Helps temporarily relieve backache pain

Removed "Helps"

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 54973-4011-1

100 TABLETS

labellabelcartoncarton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54973-4011-1Backache Relief1 in 1 CARTONTABLET14
54973-4011-1Backache Relief100 in 1 BOTTLETABLET1004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54973-4011BACKACHE RELIEF (ACONITUM NAPELLUS, BRYONIA ALBA ROOT, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, BELLIS PERENNIS, TOXICODENDRON PUBESCENS LEAF AND ARNICA MONTANA) TABLET [HYLAND'S INC.]4Current NDC, Legacy NDC, 2 package rows20230511_a51452b3-0aba-6928-e053-2995a90a1619.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54973-401154973-4011-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML · Source PDF

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
Backache ReliefACONITUM NAPELLUS, BRYONIA ALBA ROOT, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, BELLIS PERENNIS, TOXICODENDRON PUBESCENS LEAF AND ARNICA MONTANAHyland's Inc.a51452b3-0aba-6928-e053-2995a90a16192023-05-10WarningsExact identifier
ndc (package): 54973-4011-1
ndc (product): 54973-4011
ndc11 (package): 54973401101
spl id: fb5962be-5af1-206f-e053-6294a90aa8b0
spl set id: a51452b3-0aba-6928-e053-2995a90a1619

Reported adverse events (FAERS/openFDA)#

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