NDC 36800-079 Topcare Aloe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 36800 - Topco Associates Llc
- 36800-079 - Topcare
Product Packages
NDC Code 36800-079-02
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 36800-079-08
Package Description: 237 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 36800-079?
What are the uses for Topcare Aloe?
Which are Topcare Aloe UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Topcare Aloe 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:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Topcare Aloe?
- RxCUI: 582753 - ethanol 70 % Topical Solution
- RxCUI: 582753 - ethanol 0.7 ML/ML Topical Solution
- RxCUI: 582753 - ethyl alcohol 70 % Topical Solution
* 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".