NDC 52891-103 Dr. Oberon Natural Baby
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 52891-103?
Which are Dr. Oberon Natural Baby UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Dr. Oberon Natural Baby 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)
- CAPRYLIC/CAPRIC/SUCCINIC TRIGLYCERIDE (UNII: J4BY50FL78)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)
- TREHALOSE (UNII: B8WCK70T7I)
- BETAINE (UNII: 3SCV180C9W)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- SQUALANE (UNII: GW89575KF9)
- ZANTHOXYLUM PIPERITUM FRUIT PULP (UNII: 7PFC2VA251)
- PULSATILLA KOREANA WHOLE (UNII: 5R35881OBK)
- USNEA BARBATA (UNII: D6DVA9TCAP)
- CARBOMER 1342 (UNII: 809Y72KV36)
- ARGININE (UNII: 94ZLA3W45F)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PANTHENOL (UNII: WV9CM0O67Z)
- CERAMIDE 3 (UNII: 4370DF050B)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
- ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PUNICA GRANATUM WHOLE (UNII: O2ZTS50U5E)
- P-ANISIC ACID (UNII: 4SB6Y7DMM3)
- DIPOTASSIUM GLUCOSE-6-PHOSPHATE (UNII: ZZW95F4360)
- XANTHAN GUM (UNII: TTV12P4NEE)
- LAVANDULA ANGUSTIFOLIA WHOLE (UNII: 51217XIL5L)
* 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".