Zeroma7

Manufacturer
Ingenue Care Inc
Effective date
2018-10-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:56:58

Label at a glance#

ProductZeroma7
Active ingredientCAMPHOR (SYNTHETIC), PEPPERMINT OIL
Label structure8 sections

Indications and uses

Uses Aroma therapy blend essential oil for temporary relieves minor aches, pains of muscles and joints associated with: Arthritis Simple backache Strains Bruises Sprains

Dosage and administration

Adults and children 12 years of age and over: Clean and dry affected area Remove patch from film Apply to affected area no more than 3 to 4 times daily for 7 days Remove patch from skin after at most 8 hours’ application Children undress 12 years of age: consult a doctor

Label contents#

Full prescribing information#

Uses

DOSAGE & ADMINISTRATION SECTION

Uses Aroma therapy blend essential oil for temporary relieves minor aches, pains of muscles and joints associated with:

Arthritis Simple backache Strains Bruises Sprains

Warnings

WARNINGS SECTION

For external use only

Do not use on wounds or damaged skin with a heating pad

if you are allergic to any ingredients of this product

with other external analgesic products

When using this product

Use only as directed

avoid contact with eyes, mucous membranes or rashes

do not bandage tightly

Stop use and ask a doctor if

rash, itching, or excessive skin irritation develops

conditions worsen

symptoms persist for more than 7 days

symptoms clear up and occur again within a few days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

If pregnant or breast-feeding, ask a health professional before use

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Peppermint Oil 8% ------------------------------------ Topical Analgesic

Camphor Oil 8% --------------------------------------- Topical Analgesic

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Directions

INDICATIONS & USAGE SECTION

Adults and children 12 years of age and over:

Clean and dry affected area

Remove patch from film

Apply to affected area no more than 3 to 4 times daily for 7 days

Remove patch from skin after at most 8 hours’ application

Children undress 12 years of age: consult a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Gaultheria Procumbens (Wintergreen) Oil, Rosmarinus Officinalis (Rosemary) Oil, Citrus Paradisi (Grapefruit) Oil, Heterotheca Inuloides (Arnica Herbal) Oil, Aloe Vera Leaf Extract, Witch Hazel, Olive Oil, Carbomer, Water, Stearic Acid, Propylene Glycol, Isopropyl Palmitate, Cetyl Alcohol, Glycerol Stearate, Lanolin, Polymethoxy Bicyclic Oxazolidine, Mineral Oil & Lanolin Alcohol, Allantoin, Tocopherol Acetate, Aloe Vera Gel, Methyl Paraben, Urea, Potassium Hydroxide, Chloroxylenol, Propyl Paraben, Sodium Hydroxide.

Zeroma7

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZEROMA Label Review by JK 100118ZEROMA Label Review by JK 100118

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2059051camphor oil 8 % / peppermint oil 8 % Topical GelPSN2
2059051camphor oil 0.08 MG/MG / peppermint oil 0.08 MG/MG Topical GelSCD2
2059051camphor oil 8 % / peppermint oil 8 % Topical GelSY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
PEPPERMINT Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72589-100-012020-01-31C16284748780-19d75b9d0-0c25-f424-e053-dadaa90a57ceZeroma7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72589-100-01Zeroma785 g in 1 BOTTLE, PLASTICGEL852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72589-100ZEROMA7 (PEPPERMINT OIL, CAMPHOR OIL) GEL [INGENUE CARE INC]2Legacy NDC, 1 package rows20181010_77bbd207-4ec2-6fd9-e053-2991aa0a69fd.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72589-10072589-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

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
77c1c020-9172-6a35-e053-2991aa0a706d77bbd207-4ec2-6fd9-e053-2991aa0a69fd2018-10-08WarningsExact identifier
spl id: 77c1c020-9172-6a35-e053-2991aa0a706d
spl set id: 77bbd207-4ec2-6fd9-e053-2991aa0a69fd

Reported adverse events (FAERS/openFDA)#

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