NDC 62670-3756 Anti-bacterial Hand Spray Sweet Pea
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62670 - Bath & Body Works, Inc.
- 62670-3756 - Anti-bacterial Hand Spray
Product Packages
NDC Code 62670-3756-2
Package Description: 56 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 62670-3756?
What are the uses for Anti-bacterial Hand Spray Sweet Pea?
Which are Anti-bacterial Hand Spray Sweet Pea UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Anti-bacterial Hand Spray Sweet Pea 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BLACK OLIVE (UNII: 2M6QWV94OC)
- COCONUT (UNII: 3RT3536DHY)
- HONEY (UNII: Y9H1V576FH)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- AVOBENZONE (UNII: G63QQF2NOX)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTISALATE (UNII: 4X49Y0596W)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
What is the NDC to RxNorm Crosswalk for Anti-bacterial Hand Spray Sweet Pea?
- RxCUI: 1052530 - ethanol 72 % Topical Solution
- RxCUI: 1052530 - ethanol 0.72 ML/ML 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".