NDC 64942-1252 Clear Complete Care Antidandruff
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64942 - Conopco Inc. D/b/a Unilever
- 64942-1252 - Clear
Product Packages
NDC Code 64942-1252-1
Package Description: 381 mL in 1 CONTAINER
NDC Code 64942-1252-2
Package Description: 89 mL in 1 CONTAINER
NDC Code 64942-1252-3
Package Description: 50 mL in 1 CONTAINER
Product Details
What is NDC 64942-1252?
What are the uses for Clear Complete Care Antidandruff?
Which are Clear Complete Care Antidandruff UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE (UNII: 6GK82EC25D) (Active Moiety)
Which are Clear Complete Care Antidandruff 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SODIUM LAUROYL ISETHIONATE (UNII: M590021Z02)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- TEA-DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PPG-9 (UNII: I29VQH0G0B)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- NIACINAMIDE (UNII: 25X51I8RD4)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PALMITIC ACID (UNII: 2V16EO95H1)
- ZINC SULFATE (UNII: 89DS0H96TB)
- DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM ISETHIONATE (UNII: 3R36J71C17)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- LAURETH-23 (UNII: N72LMW566G)
- LAURETH-4 (UNII: 6HQ855798J)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- ALMOND OIL (UNII: 66YXD4DKO9)
- POLYETHYLENE GLYCOL 400000 (UNII: 439X29GCJZ)
- PANTHENOL (UNII: WV9CM0O67Z)
- LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM)
- HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
- SOYBEAN OIL (UNII: 241ATL177A)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
What is the NDC to RxNorm Crosswalk for Clear Complete Care Antidandruff?
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
* 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".