NDC 47046-180 My Fair Baby Oral Gel Instant Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 47046 - Anicare Pharmaceuticals Pvt. Ltd.
- 47046-180 - My Fair Baby Oral Gel
Product Packages
NDC Code 47046-180-02
Package Description: 1 TUBE in 1 BOX / 14 g in 1 TUBE (47046-180-01)
Product Details
What is NDC 47046-180?
What are the uses for My Fair Baby Oral Gel Instant Pain Relief?
Which are My Fair Baby Oral Gel Instant Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are My Fair Baby Oral Gel Instant Pain Relief 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:
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- GELATIN (UNII: 2G86QN327L)
- MINERAL OIL (UNII: T5L8T28FGP)
- PECTIN (UNII: 89NA02M4RX)
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for My Fair Baby Oral Gel Instant Pain Relief?
- RxCUI: 198496 - benzocaine 7.5 % Oral Gel
- RxCUI: 198496 - benzocaine 0.075 MG/MG Oral Gel
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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".