NDC 61995-1106 Anti Dandruff

NDC Product Code 61995-1106

NDC CODE: 61995-1106

Proprietary Name: Anti Dandruff What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

  • 61995 - The Hain Celestial Group, Inc.

NDC 61995-1106-9

Package Description: 414 g in 1 BOTTLE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Anti Dandruff with NDC 61995-1106 is a product labeled by The Hain Celestial Group, Inc.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 205104.

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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • WATER (UNII: 059QF0KO0R)
  • SODIUM COCO-SULFATE (UNII: 3599J29ANH)
  • COCO GLUCOSIDE (UNII: ICS790225B)
  • GLYCERYL OLEATE (UNII: 4PC054V79P)
  • CHAMOMILE (UNII: FGL3685T2X)
  • MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
  • ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O)
  • STYRAX BENZOIN RESIN (UNII: FE663Z8IRO)
  • CANARIUM LUZONICUM WHOLE (UNII: 5BH1ESR432)
  • CEDRUS ATLANTICA BARK OIL (UNII: ZX5QRE4U60)
  • ORANGE OIL (UNII: AKN3KSD11B)
  • LEMON OIL (UNII: I9GRO824LL)
  • COPAIFERA OFFICINALIS RESIN (UNII: 1VH544O5AT)
  • CORIANDER OIL (UNII: 7626GC95E5)
  • GERANIUM MACULATUM WHOLE (UNII: LFG25P7V8M)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)
  • MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)
  • MENTHA PIPERITA (UNII: 79M2M2UDA9)
  • POGOSTEMON CABLIN WHOLE (UNII: H6UKY25H2P)
  • ROSEMARY OIL (UNII: 8LGU7VM393)
  • .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
  • DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)
  • HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
  • INULIN (UNII: JOS53KRJ01)
  • MENTHOL (UNII: L7T10EIP3A)
  • POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
  • SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
  • SODIUM SULFATE (UNII: 0YPR65R21J)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • ALCOHOL (UNII: 3K9958V90M)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)

Product Labeler Information

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

Labeler Name: The Hain Celestial Group, Inc.
Labeler Code: 61995
Start Marketing Date: 01-29-2014 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

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Information for Patients

Salicylic Acid Topical

Salicylic Acid Topical is pronounced as (sal'' i sil' ik as' id)

Why is salicylic acid topical medication prescribed?
Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions ...
[Read More]

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Anti Dandruff Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Drug Facts

Salicylic Acid    2.0%

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