Home NDC 41163-099 Clear Anti Itch
Product NDC 41163-099
11-digit product format 411630099
Labeler code 41163
Product ID 41163-099_5aa9775d-d73c-927e-e063-6394a90a252b
Type HUMAN OTC DRUG
Nonproprietary name Pramoxine HCl, Zinc acetate
Dosage form LOTION
Route TOPICAL
Labeler United Natural Foods, Inc. dba UNFI
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-04-02
Substance PRAMOXINE HYDROCHLORIDE; ZINC ACETATE
Active strength 10; 1 mg/mL; mg/mL
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 Clear Anti Itch
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PRAMOXINE HYDROCHLORIDE 10 mg/mL ZINC ACETATE 1 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 88AYB867L5 Internal UNII lookup FM5526K07A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1234546 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 41163-099-30 Clear Anti Itch 177 mL in 1 BOTTLE, PLASTIC LOTION 177 16
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded PRAMOXINE HYDROCHLORIDE ACTIVE INGREDIENT 88AYB867L5 CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 ZINC ACETATE ACTIVE INGREDIENT FM5526K07A CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 PRAMOXINE ACTIVE MOIETY 068X84E056 CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 ZINC CATION ACTIVE MOIETY 13S1S8SF37 CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 CAMPHOR (NATURAL) INACTIVE INGREDIENT N20HL7Q941 CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 CITRIC ACID MONOHYDRATE INACTIVE INGREDIENT 2968PHW8QP CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 DIAZOLIDINYL UREA INACTIVE INGREDIENT H5RIZ3MPW4 CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 LAVENDER OIL INACTIVE INGREDIENT ZBP1YXW0H8 CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 POLYSORBATE 40 INACTIVE INGREDIENT STI11B5A2X CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 ROSEMARY OIL INACTIVE INGREDIENT 8LGU7VM393 CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 SODIUM CITRATE INACTIVE INGREDIENT 1Q73Q2JULR CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [SUPERVALU, INC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41163-099 CLEAR ANTI ITCH (PRAMOXINE HCL, ZINC ACETATE) LOTION [UNITED NATURAL FOODS, INC. DBA UNFI] 14 Current NDC, Legacy NDC, 1 package rows 20240915_242adc68-f9e0-4f69-a580-a107d1634b50.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 50 of 68 · 1,357 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Shea Butter Petroleum Jelly PETROLATUM JELLY Walgreens e35d913e-2195-4e3d-ae38-f010317140fd 2024-12-17 Warnings Exact identifier application number: M016 Jell Pharmaceuticals Vitamin A D PETROLATUM Jell Pharmaceuticals Pvt. Ltd. 6ab8ba54-3679-4fd0-a876-cb89aace96ca 2024-12-17 Warnings Exact identifier application number: M016 Shea Butter Petroleum Jelly PETROLATUM JELLY Jell Pharmaceuticals Pvt. Ltd. cd848f33-e863-d3af-e053-2a95a90a45b1 2024-12-17 Warnings Exact identifier application number: M016 Softlips Cherry, Raspberry, Vanilla DIMETHICONE The Mentholatum Company b7b2f64e-27b4-4c71-95cf-78b37540f975 2024-12-17 Warnings Exact identifier application number: M016 Softlips Tropical Coconut DIMETHICONE The Mentholatum Company 1203ea70-dc1a-4439-a230-bd3fc45f75f5 2024-12-17 Warnings Exact identifier application number: M016 Softlips Tropical Coconut Peach Passion DIMETHICONE The Mentholatum Company 11f619e7-4a58-45e4-8f4a-fe358832ab64 2024-12-17 Warnings Exact identifier application number: M016 Softlips Watermelon, Tropical Coconut, Peach Passion DIMETHICONE The Mentholatum Company e9212502-909a-4184-905e-f31a53602c3b 2024-12-17 Warnings Exact identifier application number: M016 Softlips Watermelon DIMETHICONE The Mentholatum Company e32d738e-e0af-4f17-a753-bdc7938b1684 2024-12-17 Warnings Exact identifier application number: M016 Softlips Peach Passion DIMETHICONE The Mentholatum Company 4a133e73-e51b-4f04-91de-dc8c4d4dba30 2024-12-17 Warnings Exact identifier application number: M016 Sweet Cheeks Diaper ZINC OXIDE Tubby Todd 4ed0afe1-c893-453e-b4d5-f32561360ec1 2024-12-17 Warnings Exact identifier application number: M016 White Petrolatum PETROLATUM Geri-Care Pharmaceuticals, Corp f40a29c2-65ea-91f9-e053-2a95a90ac439 2024-12-17 Warnings Exact identifier application number: M016 Vitamin A and D PETROLATUM Geri-care Pharmaceutials Corp fd76c101-a287-f92c-e053-6294a90a4468 2024-12-17 Warnings Exact identifier application number: M016 Foster and Thrive Phenolated Calamine CALAMINE AND ZINC OXIDE AND PHENOL Strategic Sourcing Services LLC 298171e1-2826-d33b-e063-6394a90a875a 2024-12-17 Warnings Exact identifier application number: M016 Secura Dimethicone Protectant DIMETHICONE Smith & Nephew Medical Ltd 83f92ac9-4114-4192-926d-be2854a84106 2024-12-16 Warnings Exact identifier application number: M016 CVS Maximum Strength Anti-Itch Cream HYDROCORTISONE 1% CVS Health c2876cba-d7e7-de5c-e053-2a95a90a6355 2024-12-16 Warnings Exact identifier application number: M016 Blistex Medicated Lip Balm Variety Pack (Blistex Medicated Berry Lip Balm, Blistex Medicated Lip Balm, Blistex Medicated Lip) DIMETHICONE, OCTINOXATE, OCTISALATE, CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND PHENOL Blistex Inc 4121d671-521c-4f36-b2db-652c13f730c6 2024-12-16 Warnings Exact identifier application number: M016 Blistex Medicated Lip Balm Variety Pack (Blistex Medicated Berry Lip Balm, Blistex Medicated Lip Balm, Blistex Medicated Mint Lip Balm) DIMETHICONE, OCTINOXATE, AND OCTISALATE Blistex Inc 24e1d2fc-3f9d-4e86-a397-61bfbfc4d58c 2024-12-16 Warnings Exact identifier application number: M016 Balmex Diaper Rash ZINC OXIDE 11.3% Randob Labs, LTD f7f7a89d-d4e0-9faa-e053-6294a90aaf7b 2024-12-15 Warnings Exact identifier application number: M016 QC Scar ALLANTOIN 0.5% CDMA f7e3d751-a47a-2bca-e053-6394a90a6541 2024-12-15 Warnings Exact identifier application number: M016 Dr. Butler Soothing Incontinence PETROLATUM 36% Beyond Health P.A. d17a0c28-a5b7-4df0-e053-2995a90a8edd 2024-12-15 Warnings Exact identifier application number: M016
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 41163-099-30 41163009930 177 mL in 1 BOTTLE, PLASTIC (41163-099-30) 177 ml 2005-04-02 0000-00-00 No No Current