Home NDC 71101-035 HealthWise Feminine Anti-itch Cream
Product NDC 71101-035
11-digit product format 711010035
Labeler code 71101
Product ID 71101-035_19fe7b4f-47ce-8c48-e063-6394a90ab211
Type HUMAN OTC DRUG
Nonproprietary name BENZOCAINE, RESORCINOL
Dosage form CREAM
Route TOPICAL
Labeler Veridian Healthcare
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-05-01
Substance BENZOCAINE; RESORCINOL
Active strength 5.67; .85 g/28g; g/28g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base HealthWise Feminine Anti-itch Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 5.67 g/28g RESORCINOL .85 g/28g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup YUL4LO94HK Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 637518 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71101-035-01 HealthWise Feminine Anti-itch Cream 28 g in 1 TUBE CREAM 28 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71101-035 HEALTHWISE FEMININE ANTI-ITCH CREAM (BENZOCAINE, RESORCINOL) CREAM [VERIDIAN HEALTHCARE] 1 Current NDC, 1 package rows 20240605_19fe7c3b-58e2-6c16-e063-6394a90a612a.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 116 of 152 · 3,029 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 71101-035-01 71101003501 28 g in 1 TUBE (71101-035-01) 28 g 2024-05-01 No No Current