NDC 69257-211 Sigform Herbal Muscle
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69257 - Signature Formulations Llc
- 69257-211 - Sigform Herbal Muscle
Product Packages
NDC Code 69257-211-21
Package Description: 90 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 69257-211?
What are the uses for Sigform Herbal Muscle?
Which are Sigform Herbal Muscle UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Sigform Herbal Muscle Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- GLYCERIN (UNII: PDC6A3C0OX)
- TRICAPRYLIN (UNII: 6P92858988)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- COCONUT OIL (UNII: Q9L0O73W7L)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- CLOVE OIL (UNII: 578389D6D0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ALLANTOIN (UNII: 344S277G0Z)
What is the NDC to RxNorm Crosswalk for Sigform Herbal Muscle?
- RxCUI: 1608801 - camphor 2 % / menthol 6 % Topical Lotion
- RxCUI: 1608801 - camphor 20 MG/ML / menthol 60 MG/ML Topical Lotion
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".