NDC 61312-003 Wet Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61312 - Hangzhou Guoguang Touring Commodity Co., Ltd.
- 61312-003 - Wet Wipes
Product Packages
NDC Code 61312-003-01
Package Description: 35 POUCH in 1 BAG / .0054 g in 1 POUCH
Product Details
What is NDC 61312-003?
What are the uses for Wet Wipes?
Which are Wet Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Wet Wipes 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DODECYL PROPIONATE (UNII: 7G537BMD9L)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM LAURAMINOPROPIONATE (UNII: X5NJA9HXPU)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TEA LEAF OIL (UNII: VC855RRT77)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PEG-40 HYDROGENATED LANOLIN (UNII: 959P5CXE48)
- TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
What is the NDC to RxNorm Crosswalk for Wet Wipes?
- RxCUI: 797892 - salicylic acid 2 % Medicated Pad
- RxCUI: 797892 - salicylic acid 20 MG/ML Medicated Pad
- RxCUI: 797892 - salicylic acid 2 % Topical Swab
* 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".