NATURAL 17 HERBAL SPLASH

Manufacturer
NATURAL 17
Effective date
2024-11-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:38:48

Label at a glance#

ProductNATURAL 17 HERBAL SPLASH
Active ingredientMENTHOL
Label structure13 sections

Dosage and administration

Adults and Children over 12 years Spray two to three pumps or as necessary to cover the affected area not more than three to four times daily. Children under 12 years of age: do not use, consult a doctor.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol …………………………………………...………………….……... 2%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

For temporary relief of minor pains on muscles and joints.

WARNINGS SECTION

For external use only.

Do not use on wounds or damaged skin, with a heating pad or on a child under 12 years of age.

Extremely flammable

USER SAFETY WARNINGS SECTION

Keep away from fire or flame.

OTC - WHEN USING SECTION

Use only as directed.
Avoid contact with eyes and mucous membranes.
If you experience an allergic reaction, discontinue use, and consult a physician.

Do not expose the area treated with product to heat or direct sunlight.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Condition worsens.
Redness is present.
Irritation develops.
Symptoms persist for more than 7 days or clear up occur again within a few days.

You experience signs injury, such as pain, swelling or blistering where the product was applied.

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help, or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 12 years

Spray two to three pumps or as necessary to cover the affected area not more than three to four times daily.

Children under 12 years of age: do not use, consult a doctor.

Other information

OTHER SAFETY INFORMATION

Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

INACTIVE INGREDIENT SECTION

Alcohol Denat, Water (Aqua), Eucalyptus Globulus Leaf Oil, Isopropyl Alcohol, Propylene Glycol, Fragrance (Parfum), Polysorbate 20, Mentha Arvensis Herb Oil, Thymus Vulgaris (Thyme) Oil, Aloe Barbadensis Leaf Extract, Glycerin, Benzyl Alcohol, Benzoic Acid, Sorbic Acid, Geraniol, Hexyl Cinnamal, Amyl Cinnamal, Citronellol, Hydroxycitronnellal, Linalool, Coumarin.

NATURAL 17 - HERBAL SPLASH

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NATURAL 17 - HERBAL SPLASHNATURAL 17 - HERBAL SPLASH

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80770-020-04NATURAL 17 HERBAL SPLASH118 mL in 1 BOTTLE, SPRAYSPRAY1182

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80770-020NATURAL 17 HERBAL SPLASH (MENTHOL) SPRAY [NATURAL 17]21 package rows20241124_056b8125-b4de-8215-e063-6394a90ab5e1.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
80770-02080770-020-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
27867af2-b4ca-1f93-e063-6394a90a8a52056b8125-b4de-8215-e063-6394a90ab5e12024-11-22WarningsExact identifier
spl id: 27867af2-b4ca-1f93-e063-6394a90a8a52
spl set id: 056b8125-b4de-8215-e063-6394a90ab5e1

Reported adverse events (FAERS/openFDA)#

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