NDC 73076-129 Petrolatum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73076 - Shenzhen Ishan Technology Co., Ltd
- 73076-129 - Petrolatum
Product Packages
NDC Code 73076-129-01
Package Description: 20 g in 1 TUBE
Product Details
What is NDC 73076-129?
What are the uses for Petrolatum?
Which are Petrolatum UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Petrolatum 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:
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- GLYCERIN (UNII: PDC6A3C0OX)
- CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
- RHUS CHINENSIS WHOLE (UNII: J6BED8187F)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- ZAOCYS DHUMNADES (UNII: SI7366N5PD)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- BORNEOL (UNII: M89NIB437X)
- CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- ARNEBIA GUTTATA ROOT (UNII: 9XN41J8M2D)
- LONICERA JAPONICA TOP (UNII: 60Q6UP226V)
- MINERAL OIL (UNII: T5L8T28FGP)
- STELLERA CHAMAEJASME WHOLE (UNII: 80N0P0DD9J)
- ALOE (UNII: V5VD430YW9)
- WATER (UNII: 059QF0KO0R)
- VIOLA PATRINII WHOLE (UNII: C1O8TSX4LG)
- DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)
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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".