NDC 52410-3060 Medpride En Shield Aloe Soft Vitamin Enriched
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52410 - Shield Line Llc
- 52410-3060 - Medpride
Product Packages
NDC Code 52410-3060-2
Package Description: 5 g in 1 PACKET
NDC Code 52410-3060-3
Package Description: 15 g in 1 PACKET
NDC Code 52410-3060-4
Package Description: 113 g in 1 TUBE
NDC Code 52410-3060-5
Package Description: 453 g in 1 JAR
Product Details
What is NDC 52410-3060?
What are the uses for Medpride En Shield Aloe Soft Vitamin Enriched?
Which are Medpride En Shield Aloe Soft Vitamin Enriched UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Medpride En Shield Aloe Soft Vitamin Enriched 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)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- CETETH-10 (UNII: LF9X1PN3XJ)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ACETATE (UNII: 4Q43814HXS)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- GLYCERIN (UNII: PDC6A3C0OX)
- LANOLIN (UNII: 7EV65EAW6H)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MINERAL OIL (UNII: T5L8T28FGP)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PETROLATUM (UNII: 4T6H12BN9U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)
- STEARETH-20 (UNII: L0Q8IK9E08)
- TROLAMINE (UNII: 9O3K93S3TK)
- VITAMIN A (UNII: 81G40H8B0T)
- WATER (UNII: 059QF0KO0R)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 21 (UNII: 08744Z6JNY)
What is the NDC to RxNorm Crosswalk for Medpride En Shield Aloe Soft Vitamin Enriched?
- RxCUI: 1427410 - zinc oxide 1.8 % Topical Cream
- RxCUI: 1427410 - zinc oxide 18 MG/ML Topical Cream
- RxCUI: 1427410 - ZNO 18 MG/ML Topical 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".