rocksauce ice

Manufacturer
Ningbo Pulisi Daily Chemical Products Co.,Ltd.
Effective date
2017-12-13
Label type
HUMAN OTC DRUG LABEL
Version
16
Source
full-release
Hydrated at
2026-05-31 22:53:25

Label at a glance#

Productrocksauce ice
Active ingredientMENTHOL
Label structure10 sections

Indications and uses

For temporary relief minor muscular discomfort

Dosage and administration

For the temporary relief of minor muscular discomfort. See important warnings under "When using this product". Not for use on children 5 years or younger. Apply liberally to painful area and massage until lotion is absorbed into the skin. Repeat 3-4 times daily. Store at 68 to 77F (20 to 25 C)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol    6%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses:

INDICATIONS & USAGE SECTION

For temporary relief minor muscular discomfort

Warnings:

WARNINGS SECTION

For external use only.

Avoid contact with eyes, mucous membrane or broken skin

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if accidentally ingested, getmedical help or contact a Poison Control Center immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

For the temporary relief of minor muscular discomfort. See important warnings under "When using this product". Not for use on children 5 years or younger. Apply liberally to painful area and massage until lotion is absorbed into the skin. Repeat 3-4 times daily. Store at 68 to 77F (20 to 25 C)

When using this product

OTC - WHEN USING SECTION

do not heat, microwave, and to hot water or any container where heating water may cause splattering and result in burns, use in eyes or directly on mucus membrans, take by mouth or place in nostrill, apply to wounds or damaged skin. Do not use otherwise than as directed

Consult a doctor and discontinus use.

OTC - STOP USE SECTION

if conditions persist for more than 1 week or reocur.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

2-amino-2-methyl-1-propanol, Aloe barbadensis (aloe vera) Leaf Extract, Arnica Montana Extract, Carbomer, Cetearyl Alcohol, Ethylhexylglycerin, Ethylhexyl, Palmitate, Glycerin, Methylisothiazolinone, Propylene Glycol, Tocopheryl Acetate, Water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label
label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1488306menthol 6 % Topical CreamPSN16
1488306menthol 60 MG/ML Topical CreamSCD16
1488306menthol 6 % Topical CreamSY16

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
40104-299-012020-01-31C16284748780-19d75b9d0-16c9-f424-e053-dadaa90a57cerock sauce for temporary relief of muscle aches and pains

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
40104-299-01rocksauce ice1 in 1 PACKAGECREAM116
40104-299-01rocksauce ice2.5 g in 1 BOTTLECREAM2.516

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
40104-299ROCKSAUCE ICE (MENTHOL) CREAM [NINGBO PULISI DAILY CHEMICAL PRODUCTS CO.,LTD.]16Legacy NDC, 2 package rows20171213_c46a6f07-79aa-40d9-9413-6c1a836a3be4.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
40104-29940104-299-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
d8eaf690-7aef-43fb-8e87-c6b9d31c3a84c46a6f07-79aa-40d9-9413-6c1a836a3be42017-12-13WarningsExact identifier
spl id: d8eaf690-7aef-43fb-8e87-c6b9d31c3a84
spl set id: c46a6f07-79aa-40d9-9413-6c1a836a3be4

Reported adverse events (FAERS/openFDA)#

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