NDC 76751-311 Olika Hand Sanitizer Charcoal

Ethyl Alcohol

NDC Product Code 76751-311

NDC 76751-311-01

Package Description: 30 mL in 1 BOTTLE, PUMP

NDC 76751-311-02

Package Description: 20 mL in 1 BOTTLE, PUMP

NDC 76751-311-03

Package Description: 90 mL in 1 POUCH

NDC Product Information

Olika Hand Sanitizer Charcoal with NDC 76751-311 is a a human over the counter drug product labeled by Perkin And Perkin Llc. The generic name of Olika Hand Sanitizer Charcoal is ethyl alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Perkin And Perkin Llc

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Olika Hand Sanitizer Charcoal Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL 65.1846 mL/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • 2,6-DIMETHYL-5-HEPTENAL (UNII: Z331YX9EL9)
  • .DELTA.-DECALACTONE (UNII: CNA0S5T234)
  • PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
  • VANILLIN (UNII: CHI530446X)
  • CARDAMOM OIL (UNII: JM0KJ091HZ)
  • METHYL ANTHRANILATE (UNII: 981I0C1E5W)
  • CITRUS SINENSIS LEAF (UNII: VF01D90MZI)
  • CANANGA ODORATA FLOWER (UNII: 76GTF6Z97M)
  • .GAMMA.-OCTALACTONE (UNII: UHD6M52X0K)
  • BERGAMOT OIL (UNII: 39W1PKE3JI)
  • POGOSTEMON CABLIN LEAF OIL (UNII: F3IN55X5PO)
  • .GAMMA.-DECALACTONE (UNII: 7HLS05KP9O)
  • MANDARIN OIL (UNII: NJO720F72R)
  • CLOVE LEAF OIL (UNII: VCA5491KVF)
  • CITRUS SINENSIS FLOWER OIL (UNII: AJ56JP5TFP)
  • ALLYL HEXANOATE (UNII: 3VH84A363D)
  • LEMON OIL (UNII: I9GRO824LL)
  • PIPERONAL (UNII: KE109YAK00)
  • PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
  • CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
  • TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
  • LINALOOL, (-)- (UNII: 3U21E3V8I2)
  • .ALPHA.-TERPINEOL (UNII: 21334LVV8W)
  • PALMAROSA OIL (UNII: 0J3G3O53ST)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • WATER (UNII: 059QF0KO0R)
  • MALTOL (UNII: 3A9RD92BS4)
  • .DELTA.-DODECALACTONE (UNII: 33DIC582TL)
  • BENZYL SALICYLATE (UNII: WAO5MNK9TU)
  • LITSEA OIL (UNII: 2XIW34BN6O)
  • ORANGE OIL (UNII: AKN3KSD11B)
  • SPEARMINT OIL (UNII: C3M81465G5)
  • DIPTERYX ODORATA SEED (UNII: D43A5L1U6L)
  • VANILLIN (UNII: CHI530446X)
  • TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
  • LAVANDIN OIL (UNII: 9RES347CKG)
  • LEMON OIL (UNII: I9GRO824LL)
  • LINALOOL, (-)- (UNII: 3U21E3V8I2)
  • AMYRIS BALSAMIFERA OIL (UNII: I1BJ961J2E)
  • POGOSTEMON CABLIN LEAF OIL (UNII: F3IN55X5PO)
  • BULNESIA SARMIENTOI WOOD OIL (UNII: 81H0L6W02F)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)
  • JUNIPERUS DEPPEANA WOOD OIL (UNII: 4739QA5686)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • WATER (UNII: 059QF0KO0R)
  • LEMON OIL (UNII: I9GRO824LL)
  • CLARY SAGE OIL (UNII: 87L0D4U3M0)
  • BERGAMOT OIL (UNII: 39W1PKE3JI)
  • VETIVER OIL (UNII: 9M9P32M01L)
  • TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
  • POGOSTEMON CABLIN LEAF OIL (UNII: F3IN55X5PO)
  • AMYRIS BALSAMIFERA OIL (UNII: I1BJ961J2E)
  • BENZYL ACETATE (UNII: 0ECG3V79ZJ)
  • LABDANUM OIL (UNII: 67GS9BGA2X)
  • .BETA.-IONONE (UNII: A7NRR1HLH6)
  • BENZOIN RESIN (UNII: GK21SBA74R)
  • LINALYL ACETATE (UNII: 5K47SSQ51G)
  • JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • WATER (UNII: 059QF0KO0R)
  • LINALOOL, (-)- (UNII: 3U21E3V8I2)
  • VANILLIN (UNII: CHI530446X)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Perkin And Perkin Llc
Labeler Code: 76751
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 06-01-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

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