NDC 70118-002 Painkoolers Topical Analgesic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70118 - Ga Health And Beauty (foshan) Co., Ltd
- 70118-002 - Painkoolers Topical Analgesic
Product Packages
NDC Code 70118-002-05
Package Description: 5 PATCH in 1 POUCH / 8 g in 1 PATCH
Product Details
What is NDC 70118-002?
What are the uses for Painkoolers Topical Analgesic?
Which are Painkoolers Topical Analgesic UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
Which are Painkoolers Topical Analgesic 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- TARTARIC ACID (UNII: W4888I119H)
- DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- KAOLIN (UNII: 24H4NWX5CO)
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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".