NDC 70576-001 Pain Relief Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70576 - Health Town Inc
- 70576-001 - Pain Relief Cream
Product Packages
NDC Code 70576-001-01
Package Description: 30 g in 1 TUBE
Product Details
What is NDC 70576-001?
What are the uses for Pain Relief Cream?
Which are Pain Relief Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
Which are Pain Relief Cream 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:
- MINERAL OIL (UNII: T5L8T28FGP)
- ETHYLPARABEN (UNII: 14255EXE39)
- TROLAMINE (UNII: 9O3K93S3TK)
- ILEX PUBESCENS ROOT (UNII: V5V22LFX73)
- PHERETIMA ASPERGILLUM (UNII: 1842H27PGA)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ARALIA CHINENSIS WHOLE (UNII: 4048809221)
- OLDENLANDIA DIFFUSA (UNII: 291PPU5K9I)
- PINUS MASSONIANA LEAF (UNII: OFD5T4515T)
- AMPELOPSIS GLANDULOSA VAR. BREVIPEDUNCULATA FRUIT (UNII: Y6SZ1HB5NG)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
- LANOLIN (UNII: 7EV65EAW6H)
- MACLURA COCHINCHINENSIS ROOT (UNII: 3WTU9E1VPU)
- PETROLATUM (UNII: 4T6H12BN9U)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- DRYNARIA FORTUNEI ROOT (UNII: 731W842X8Q)
- ADINA RUBELLA ROOT (UNII: UUJ7O41XPT)
What is the NDC to RxNorm Crosswalk for Pain Relief Cream?
- RxCUI: 1746464 - camphor 1 % Topical Cream
- RxCUI: 1746464 - camphor 10 MG/ML Topical Cream
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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".