NDC 69142-001 Breast Essence Ii
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69142 - Yeojaya
- 69142-001 - Breast Essence Ii
Product Packages
NDC Code 69142-001-02
Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 50 mL in 1 BOTTLE, WITH APPLICATOR (69142-001-01)
Product Details
What is NDC 69142-001?
What are the uses for Breast Essence Ii?
Which are Breast Essence Ii UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Breast Essence Ii 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ANEMARRHENA ASPHODELOIDES WHOLE (UNII: OH50MKZ7H3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CETYL STEARATE (UNII: 06RI5UQA7L)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- BETAINE (UNII: 3SCV180C9W)
- ARBUTIN (UNII: C5INA23HXF)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- MACADAMIA OIL (UNII: 515610SU8C)
- JOJOBA OIL (UNII: 724GKU717M)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- TROLAMINE (UNII: 9O3K93S3TK)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- ADENOSINE (UNII: K72T3FS567)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- SOYBEAN SEED OIL (UNII: P6C7NVO1UF)
- PURSLANE (UNII: M6S840WXG5)
* 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".