NDC 59663-100 Rock Sauce

NDC Product Code 59663-100

NDC 59663-100-01

Package Description: 120 mL in 1 BOTTLE

NDC 59663-100-02

Package Description: 240 mL in 1 BOTTLE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Rock Sauce with NDC 59663-100 is a product labeled by Shine & Pretty (usa), Corp.. The generic name of Rock Sauce is . The product's dosage form is and is administered via form.

Labeler Name: Shine & Pretty (usa), Corp.

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • CARBOMER 934 (UNII: Z135WT9208)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Shine & Pretty (usa), Corp.
Labeler Code: 59663
Start Marketing Date: 06-02-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Rock Sauce Product Label Images

Rock Sauce Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Purpose

Uses: Temporarily relives minor muscular discomfort

Indications & Usage

When using this product, do not: heat, microwave, add to hot water or any container where heating water may cause splatterring and result in burns, use in eyes or directly on mucus membrane, take by month or place in nostrils, apply to wounds or damaged skin.


Warnings: For external use only. Avoid contact with eyes. Ask a doctor before use if you have a cough associated with smoking, excessive phlegm, asthma, emphysema, persistent or chronic cough.

Dosage & Administration

Directions: 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.

Inactive Ingredient

Inactive Ingredients: D. I. Water, Ethylhexyl Palmitate, Cetearyl Alcohol, Glycerin, Propylene Glycol, Arnica Extract, Aloe Barbadensis (Aloe Vera) Leaf Extract, Vitamin E Acetate, Carbomer, Triethanolamine, Phenoxyethanol and Methyldibrome Glutarontrile

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children: In case of accidental ingestions, get medical help or call Poison Control Center right away.

Otc - Active Ingredient

Active IngredientMethyl Salicylate   20%Menthol     10% Capsicum   0.05%

Information For Patients

Consult a doctor and discontinue use: If conditions persist for more than 1 week or reoccur.

* Please review the disclaimer below.