NDC 11673-572 Glycerin, Phenylephrine Hydrochloride, Pramoxine, White Petrolatum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11673 - Target Corporation
- 11673-572 - Glycerin, Phenylephrine Hydrochloride, Pramoxine, White Petrolatum
Product Packages
NDC Code 11673-572-24
Package Description: 1 TUBE, WITH APPLICATOR in 1 BOX / 51 g in 1 TUBE, WITH APPLICATOR
Product Details
What is NDC 11673-572?
What are the uses for Glycerin, Phenylephrine Hydrochloride, Pramoxine, White Petrolatum?
Which are Glycerin, Phenylephrine Hydrochloride, Pramoxine, White Petrolatum UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Glycerin, Phenylephrine Hydrochloride, Pramoxine, White 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LAURETH-23 (UNII: N72LMW566G)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- PANTHENOL (UNII: WV9CM0O67Z)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Glycerin, Phenylephrine Hydrochloride, Pramoxine, White Petrolatum?
- RxCUI: 1293649 - glycerin 14.4 % / phenylephrine HCl 0.25 % / pramoxine HCl 1 % / white petrolatum 15 % Rectal Cream
- RxCUI: 1293649 - glycerin 144 MG/ML / petrolatum 150 MG/ML / phenylephrine hydrochloride 2.5 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal Cream
- RxCUI: 1293649 - glycerin 14.4 % / phenylephrine hydrochloride 0.25 % / pramoxine hydrochloride 1 % / white petrolatum 15 % Rectal Cream
* 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".