NDC 76150-244 Big Cloud Defend Hybrid Formula With Zinc
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76150 - Bell International Laboratories, Inc.
- 76150-244 - Big Cloud Defend
Product Packages
NDC Code 76150-244-48
Package Description: 170 g in 1 CAN
Product Details
What is NDC 76150-244?
What are the uses for Big Cloud Defend Hybrid Formula With Zinc?
Which are Big Cloud Defend Hybrid Formula With Zinc UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Big Cloud Defend Hybrid Formula With Zinc 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- LEVOMENOL (UNII: 24WE03BX2T)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
- RICE BRAN (UNII: R60QEP13IC)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PRICKLY PEAR FRUIT (UNII: 18V8PAQ629)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- RASPBERRY SEED OIL (UNII: 9S8867952A)
- PROPANEDIOL (UNII: 5965N8W85T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ROSEMARY (UNII: IJ67X351P9)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- SHEA BUTTER (UNII: K49155WL9Y)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- WATER (UNII: 059QF0KO0R)
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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".