NDC 55560-0101 Andalou Bb Untinted With Spf-30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55560 - Andalou Naturals
- 55560-0101 - Andalou Bb Untinted With Spf-30
Product Packages
NDC Code 55560-0101-1
Package Description: 58 mL in 1 TUBE
Product Details
What is NDC 55560-0101?
What are the uses for Andalou Bb Untinted With Spf-30?
Which are Andalou Bb Untinted With Spf-30 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 Andalou Bb Untinted With Spf-30 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:
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SAGE (UNII: 065C5D077J)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- WILLOW BARK (UNII: S883J9JDYX)
- POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- MANDARIN OIL (UNII: NJO720F72R)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- JOJOBA OIL (UNII: 724GKU717M)
- TOCOPHEROL (UNII: R0ZB2556P8)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PALMAROSA OIL (UNII: 0J3G3O53ST)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
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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".