NDC 43251-3213 Natralia Cramp Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43251 - Laderma Trading Pty Ltd
- 43251-3213 - Natralia Cramp Relief
Product Packages
NDC Code 43251-3213-3
Package Description: 1 TUBE in 1 CARTON / 56 g in 1 TUBE
NDC Code 43251-3213-4
Package Description: 3 g in 1 PACKET
Product Details
What is NDC 43251-3213?
What are the uses for Natralia Cramp Relief?
Which are Natralia Cramp Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYL SALICYLATE (UNII: LAV5U5022Y) (Active Moiety)
Which are Natralia Cramp Relief 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ALCOHOL (UNII: 3K9958V90M)
- CORYMBIA CITRIODORA LEAF OIL (UNII: M63U6N96EB)
- SQUALANE (UNII: GW89575KF9)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Natralia Cramp Relief?
- RxCUI: 1094875 - methyl salicylate 10.5 % Topical Gel
- RxCUI: 1094875 - methyl salicylate 0.105 MG/MG Topical Gel
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[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".