good sense itch relief
- Product NDC
- 0113-0622
- 11-digit product format
- 001130622
- Labeler code
- 0113
- Product ID
- 0113-0622_fefc6043-624b-49b9-b2c2-da42a16bcfab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride, Zinc Acetate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- L. Perrigo Company
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2006-07-18
- 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
- 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
- good sense itch relief
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 2 g/100g |
| ZINC ACETATE | .1 g/100g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| TC2D6JAD40 | Internal UNII lookup |
| FM5526K07A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1087026 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 162fe0a3-3995-4e6f-94ed-f839b2b0c80e | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f47a510b-6679-4664-b2d6-47b5c4afe7cc | Product name | 4 | 20260217 |
| 030ce964-9b2d-45aa-b5d3-f78ce03ef61c | Product name | 2 | 20250515 |
| 0e2e0f88-b076-afe1-4bdd-32bca4375bec | Product name | 3 | 20250127 |
| 0306390c-dd77-4363-afe0-63c58088b2a1 | Product name | 1 | 20220120 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| 190f2a5b-bbc8-65c7-fcb0-97891307b917 | Product name | 1 | 20140508 |
| 3e48c9c4-918d-5d23-2f0b-d2398b06be54 | Product name | 1 | 20140508 |
| 865c72dd-0d94-daac-f728-ddd4ded2a79e | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0113-0622-64 | good sense itch relief | 28 g in 1 TUBE | CREAM | 28 | 3 | |
| 0113-0622-64 | good sense itch relief | 1 in 1 CARTON | CREAM | 1 | 3 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0113-0622-64 | GM - Gram | 0113-0622 | 871e4197-28c4-472f-8448-fddb226a0a75 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
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.
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1087026 | diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Cream | PSN | 162fe0a3-3995-4e6f-94ed-f839b2b0c80e | 3 |
| 1087026 | diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Cream | SCD | 162fe0a3-3995-4e6f-94ed-f839b2b0c80e | 3 |
| 1087026 | diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Cream | SY | 162fe0a3-3995-4e6f-94ed-f839b2b0c80e | 3 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0113-0622-64 | 00113062264 | 1 TUBE in 1 CARTON (0113-0622-64) / 28 g in 1 TUBE | 1 tube | 2006-07-18 | 0000-00-00 | No | No | Current |