Label: GOOD NEIGHBOR PHARMACY SCALP RELIEF- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 24385-678-27 - Packager: AmerisourceBergen Drug Corportaion
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 22, 2015
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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Works fast to help relieve
“Deep Scalp Itch”
& to help control flaking
Seborrheic dermatitis causes an intense itching condition
called “Deep Scalp Itch.” This special formula helps to
relieve deep scalp itch and control flaking. Scalp Relief may
be used after shampooing or anytime in between. After
shampooing, towel dry hair and scalp. Apply directly to your
scalp according to the directions below. Massage gently to
cover all affected areas. Scalp Relief will dry on contact, and
won’t interfere with your normal hairstyle or grooming.
Uses
Relieves and controls the following symptoms associated with
dandruff, seborrheic dermatitis and psoriasis
• scalp itching • flaking • irritation • redness • scaling
Stop use and consult a doctor
• if condition worsens or does not improve with regular use
of this product as directed
When using this product
• avoid contact with eyes. If contact occurs, rinse eyes
thoroughly with water
Keep out of the reach of children.
If swallowed get medical help or contact a Poison Control Center right away.
If pregnant or breast-feeding consult a health care professional before use.
- Good Neighbor Pharmacy Scalp Relief
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INGREDIENTS AND APPEARANCE
GOOD NEIGHBOR PHARMACY SCALP RELIEF
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24385-678 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 3 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) MENTHOL (UNII: L7T10EIP3A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALCOHOL (UNII: 3K9958V90M) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24385-678-27 3 g in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 02/02/1998 Labeler - AmerisourceBergen Drug Corportaion (007914906) Establishment Name Address ID/FEI Business Operations Product Quest Mfg, LLC 927768135 manufacture(24385-678) , label(24385-678)
