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NDC 63868-0952-02 Quality Choice Itch Relief 2; .1 g/100mL; g/100mL Details
Quality Choice Itch Relief 2; .1 g/100mL; g/100mL
Quality Choice Itch Relief is a TOPICAL SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by Chain Drug Marketing Association. The primary component is DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE.
MedlinePlus Drug Summary
Diphenhydramine is used to relieve red, irritated, itchy, watery eyes; sneezing; and runny nose caused by hay fever, allergies, or the common cold. Diphenhydramine is also used to relieve cough caused by minor throat or airway irritation. Diphenhydramine is also used to prevent and treat motion sickness, and to treat insomnia (difficulty falling asleep or staying asleep). Diphenhydramine is also used to control abnormal movements in people who have early stage parkinsonian syndrome (a disorder of the nervous system that causes difficulties with movement, muscle control, and balance) or who are experiencing movement problems as a side effect of a medication. Diphenhydramine will relieve the symptoms of these conditions but will not treat the cause of the symptoms or speed recovery. Diphenhydramine should not be used to cause sleepiness in children. Diphenhydramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
Related Packages: 63868-0952-02Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Diphenhydramine
Product Information
NDC | 63868-0952 |
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Product ID | 63868-952_8735c96c-f943-49fd-e053-2a91aa0a17db |
Associated GPIs | |
GCN Sequence Number | 029879 |
GCN Sequence Number Description | allantoin/onion/peg/water GEL (GRAM) TOPICAL |
HIC3 | L2A |
HIC3 Description | EMOLLIENTS |
GCN | 77641 |
HICL Sequence Number | 015099 |
HICL Sequence Number Description | ALLANTOIN/ONION/POLYETHYLENE GLYCOL/WATER |
Brand/Generic | Generic |
Proprietary Name | Quality Choice Itch Relief |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Diphenhydramine HCl, Zinc Acetate |
Product Type | HUMAN OTC DRUG |
Dosage Form | SPRAY |
Route | TOPICAL |
Active Ingredient Strength | 2; .1 |
Active Ingredient Units | g/100mL; g/100mL |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
Labeler Name | Chain Drug Marketing Association |
Pharmaceutical Class | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH NOT FINAL |
Application Number | part348 |
Listing Certified Through | 2024-12-31 |
Package
Package Images

NDC 63868-0952-02 (63868095202)
NDC Package Code | 63868-952-02 |
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Billing NDC | 63868095202 |
Package | 59 mL in 1 BOTTLE, SPRAY (63868-952-02) |
Marketing Start Date | 2014-04-14 |
NDC Exclude Flag | N |
Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 8735b298-83f3-0b5d-e053-2a91aa0a8292 Details
Active Ingredient
Uses
Directions
Warnings
For external use only
Do not Use
on large areas of the body
with any other product containing diphenhydramine, even one taken by mouth
Stop Use and ask physician
condition worsens
symptoms last more than 7 days or clear up and occur again within a few days
Prinicpal dispaly panel
INGREDIENTS AND APPEARANCE
QUALITY CHOICE ITCH RELIEF
diphenhydramine hcl, zinc acetate spray |
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Labeler - Chain Drug Marketing Association (011920774) |
Registrant - Weeks & LEO, Inc. (005290028) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
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Weeks & Leo | 005290028 | manufacture(63868-952) |