Home NDC 21130-154 signature care itch relief
Product NDC 21130-154
11-digit product format 211300154
Labeler code 21130
Product ID 21130-154_4e0a1cc6-292f-46d7-a5a1-0b8b642ca8fd
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine Hydrochloride, Zinc Acetate
Dosage form CREAM
Route TOPICAL
Labeler Safeway
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-09-01
Substance DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Active strength 2; .1 g/100g; g/100g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
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 signature care itch relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 2 g/100g ZINC ACETATE .1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination TC2D6JAD40 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 1087026 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 21130-154-64 signature care itch relief 1 in 1 CARTON CREAM 1 3 21130-154-64 signature care itch relief 28 g in 1 TUBE CREAM 28 3
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DIPHENHYDRAMINE HYDROCHLORIDE ACTIVE INGREDIENT TC2D6JAD40 SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1 ZINC ACETATE ACTIVE INGREDIENT FM5526K07A SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1 DIPHENHYDRAMINE ACTIVE MOIETY 8GTS82S83M SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1 ZINC CATION ACTIVE MOIETY 13S1S8SF37 SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1 CETYL ALCOHOL INACTIVE INGREDIENT 936JST6JCN SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1 DIAZOLIDINYL UREA INACTIVE INGREDIENT H5RIZ3MPW4 SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1 PEG-2 STEARATE INACTIVE INGREDIENT 94YQ11Y95F SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1 PEG-20 STEARATE INACTIVE INGREDIENT NBX892EA57 SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1 WATER INACTIVE INGREDIENT 059QF0KO0R SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21130-154 SIGNATURE CARE ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [SAFEWAY] 3 Current NDC, Legacy NDC, 2 package rows 20241015_3eedcd9f-8312-4d14-a0fe-6b00a00d3e73.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 124 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Eagle Medicated MENTHOL METHYL SALICYLATE Eagle Indo Pharma, PT da338796-de9c-be51-e053-2a95a90a2509 2024-10-07 Warnings Exact identifier application number: M017 Eagle Medicated MENTHOL METHYL SALICYLATE Eagle Indo Pharma e2c5f821-cdd5-190d-e053-2a95a90a9159 2024-10-07 Warnings Exact identifier application number: M017 NanoXtreme Pain Relieving MENTHOL, METHYL SALICYLATE MG Science Technologies LLC c1490c30-a9db-4120-adaf-9e8000169e46 2024-10-07 Warnings Exact identifier application number: M017 CAREALL Hydrocortisone Maximum Strength HYDROCORTISONE New World Imports, Inc ea656cf8-cad5-4fa5-82e7-daec77a0bb04 2024-10-07 Warnings Exact identifier application number: M017 Eagle Medicated Oil Refreshing MENTHOL, METHYL SALICYLATE Eagle Indo Pharma, PT e2729023-d689-7ae2-e053-2a95a90a78dc 2024-10-06 Warnings Exact identifier application number: M017 Flanax Back Pain Relief LIDOCAINE Belmora LLC 46d33346-e582-4af1-b81a-feca7033dceb 2024-10-04 Warnings Exact identifier application number: M017 Muscle Balm MENTHOL, UNSPECIFIED FORM, CAMPHOR (SYNTHETIC) Natural Essentials, Inc. 16918ba3-2e07-4232-9ed3-4c7751796cd2 2024-10-04 Warnings Exact identifier application number: M017 Fast Freeze Pain Relieving Continuous MENTHOL, UNSPECIFIED FORM Natural Essentials, Inc. 998a4824-9ed9-4fe0-b45b-72e52861fcd3 2024-10-04 Warnings Exact identifier application number: M017 Fast Freeze Lidocaine Roll-On LIDOCAINE HYDROCHLORIDE, BENZYL ALCOHOL Natural Essentials, Inc. 74b06366-5eb4-4eba-aa2b-2b672828294d 2024-10-04 Warnings Exact identifier application number: M017 Fast Freeze Lidocaine LIDOCAINE Natural Essentials, Inc. 029bd3fb-1b5b-48e0-b9af-d91d548b5b0f 2024-10-04 Warnings Exact identifier application number: M017 Fast Freeze MENTHOL Natural Essentials Inc. a96e3e41-871c-4cf3-93b6-af2a6246ded8 2024-10-04 Warnings Exact identifier application number: M017 CVS Pain Relief MENTHOL 4% CVS 20234356-5e80-b79e-e063-6294a90a2ee3 2024-10-04 Warnings Exact identifier application number: M017 FLANAX BACK PAIN RELIEF LIDOCAINE Belmora Llc af4bf57c-f250-4506-83eb-e0f253e96062 2024-10-04 Warnings Exact identifier application number: M017 topcare hydrocortisone HYDROCORTISONE Topco Associates LLC 11a30ec9-ebc2-4a00-8a8d-431d0d973b37 2024-10-03 Warnings Exact identifier application number: M017 pain relief patch LIDOCAINE 4% Bionpharma Inc. 19c69983-4e78-8ec5-e063-6394a90a84be 2024-10-03 Warnings Exact identifier application number: M017 Good Sense Anti Itch HYDROCORTISONE L. Perrigo Company ecd6d841-40b9-42c9-825d-d172cd04824d 2024-10-03 Warnings Exact identifier application number: M017 Gold Bond Medicated Original Strength Body MENTHOL Navajo Manufacturing Company Inc. f71d598c-92c3-d6fd-e053-6394a90a97d7 2024-10-03 Warnings Exact identifier application number: M017 Signature Care Hydrocortisone HYDROCORTISONE Safeway 9e663535-4acc-4b37-acae-8c17517c5a3d 2024-10-03 Warnings Exact identifier application number: M017 Topcare Hydrocortisone HYDROCORTISONE Topco Associates LLC 849c60fc-e455-4c50-8adf-ac59c0ee785b 2024-10-03 Warnings Exact identifier application number: M017 rexall anti itch maximum strength relief HYDROCORTISONE Dolgencorp, LLC 894cf9ab-693a-4210-96df-605947f51b63 2024-10-03 Warnings Exact identifier application number: M017
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 21130-154-64 21130015464 1 TUBE in 1 CARTON (21130-154-64) / 28 g in 1 TUBE 1 tube 2015-09-01 0000-00-00 No No Current