Home NDC 71644-010 Ava Isa Sun Lip Sun Whip
Product NDC 71644-010
11-digit product format 716440010
Labeler code 71644
Product ID 71644-010_48326f62-4953-fcd3-e063-6294a90a9fef
Type HUMAN OTC DRUG
Nonproprietary name Zinc oxide
Dosage form CREAM
Route TOPICAL
Labeler Cyberderm Laboratories inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-06-18
Substance ZINC OXIDE
Active strength 20 g/100mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2027-12-31
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 Ava Isa Sun Lip Sun Whip
Brand name suffix Strawberry Zinnia
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 20 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71644-010-10 Ava Isa Sun Lip Sun WhipStrawberry Zinnia 1 in 1 CARTON CREAM 1 6 71644-010-10 Ava Isa Sun Lip Sun WhipStrawberry Zinnia 10 mL in 1 TUBE CREAM 10 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71644-010 AVA ISA SUN LIP SUN WHIP STRAWBERRY ZINNIA (ZINC OXIDE) CREAM [CYBERDERM LABORATORIES INC.] 3 Current NDC, Legacy NDC, 2 package rows 20231128_a888396f-489f-7e7c-e053-2995a90aee5b.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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71644-010-10 71644001010 1 TUBE in 1 CARTON (71644-010-10) / 10 mL in 1 TUBE 1 tube 2020-06-19 0000-00-00 No No Current