Gold Bond Medicated Anti-Itch
- Product NDC
- 84714-0507
- 11-digit product format
- 847140507
- Labeler code
- 84714
- Product ID
- 84714-0507_40fadefc-707b-4832-8aa6-00d76ac68cbd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pramoxine Hydrochloride, Menthol
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Gold Bond Co LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-04-26
- Substance
- MENTHOL; PRAMOXINE HYDROCHLORIDE
- Active strength
- .5; 1 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Gold Bond Medicated Anti-Itch
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | .5 g/100g |
| PRAMOXINE HYDROCHLORIDE | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A, 88AYB867L5 |
| Rxcui | 1293905 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84714-0507-0 | Gold Bond Medicated Anti-Itch | 155 g in 1 BOTTLE | LOTION | 155 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84714-0507-0 | 84714050700 | 155 g in 1 BOTTLE (84714-0507-0) | 155 g | 2016-04-26 | No | No | Historical |