HEB Medicated Cornstarch Body Powder
- Product NDC
- 42669-217
- 11-digit product format
- 426690217
- Labeler code
- 42669
- Product ID
- 42669-217_d07cb2d2-d35b-4fb8-b467-b6243e4299fc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Davion, Inc
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-08-22
- Substance
- MENTHOL
- Active strength
- .15 g/100g
- 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
- HEB Medicated Cornstarch Body Powder
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MENTHOL | .15 g/100g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| L7T10EIP3A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1431703 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| df1331fb-48df-4f21-8564-0468078fd12d | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 42669-217-10 | 2024-02-28 | C162847 | 48780-1 | 1030e365-2254-111a-e063-dadaa90a10e2 | H-E-B Medicated Cornstarch Body Powder Triple Relief Formula |
| 42669-217-10 | 2024-01-30 | C162847 | 48780-1 | 1030e365-2254-111a-e063-dadaa90a10e2 | H-E-B Medicated Cornstarch Body Powder Triple Relief Formula |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 42669-217-10 | HEB Medicated Cornstarch Body Powder | 283 g in 1 BOTTLE | POWDER | 283 | 4 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| SUPER WHITE STUFF Pain Relief | MENTHOL | BLUE SPRING WELLNESS | e6d27df5-118c-4c6d-86e8-7b4401a39c76 | 2024-01-23 | Warnings | M017 |
| Burn First Aid | BURN FIRST AID | Dynarex Corporation | 826e08be-dffa-5a27-e053-2a91aa0a8701 | 2024-01-22 | Warnings | M017 |
| Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On | MENTHOL | TARGET CORPORATION | 0f95fc55-8665-9e89-e063-6394a90a7891 | 2024-01-22 | Warnings | M017 |
| CVS Health Lidocaine Pain Relief Plus Menthol | LIDOCAINE, MENTHOL, UNSPECIFIED FORM | Natural Essentials, Inc. | 77978069-a1b4-473e-83c9-8320e00eea89 | 2024-01-19 | Warnings | M017 |
| ZIMS MAX FREEZE LEG CRAMPS | CAMPHOR, MENTHOL | KOBAYASHI Healthcare International, Inc. | ba26635d-95d3-4d88-93cc-1fd4fd29fd79 | 2024-01-18 | Warnings | M017 |
| Burn | LIDOCAINE | HART Health | e95ebdac-9789-41c2-97da-2307e4538794 | 2024-01-18 | Warnings | M017 |
| Medi-First Hydrocortisone 1% | HYDROCORTISONE ACETATE | Unifirst First Aid Corporation | bd216f5d-f304-7d8d-e053-2a95a90aa9ce | 2024-01-17 | Warnings | M017 |
| Green Guard Hydrocortisone 1% | HYDROCORTISONE | Unifirst First Aid Corporation | bd348e2a-57b1-3f17-e053-2a95a90a8bdc | 2024-01-17 | Warnings | M017 |
| Pain Relief | LIDOCAINE, MENTHOL | HUMN Pharmaceuticals Inc | 6c96f94a-e724-eab3-e053-2991aa0aab88 | 2024-01-17 | Warnings | M017 |
| CVS Health Lidocaine Pain Relief | LIDOCAINE | Natural Essentials, Inc. | 52e82e70-53b7-4ecb-be39-fe10c94cc444 | 2024-01-17 | Warnings | M017 |
| CVS Health XL Lidocaine Pain Relief | LIDOCAINE | NATURAL ESSENTIALS, INC. | ec16da91-8244-402b-b8d8-84896094ac2c | 2024-01-17 | Warnings | M017 |
| Anti-itch | DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE | Target Corporation | f444b0a6-2ed3-4236-8206-342150290675 | 2024-01-17 | Warnings | M017 |
| Maximum Strength Hydrocortisone Anti-itch | HYDROCORTISONE 1% | Target Corporation | 4ff39cb8-3a20-4fe7-9829-1e882a484668 | 2024-01-17 | Warnings | M017 |
| Burn | LIDOCAINE HYDROCHLORIDE | Nantong Health & Beyond Hygienic Products Inc. | eca272cb-ac8f-982b-e053-2995a90aa8b2 | 2024-01-15 | Warnings | M017 |
| American Safety and First Aid | HYDROCORTISONE ACETATE | Orazen Inc | eb0cfde0-c463-e9b5-e053-2a95a90a1924 | 2024-01-15 | Warnings | M017 |
| American Safety and First Aid | HYDROCORTISONE ACETATE | Orazen Inc | eb0cce4b-c70a-1b2d-e053-2995a90aa4aa | 2024-01-15 | Warnings | M017 |
| Oral Pain Relief Gel | BENZOCAINE 20% | Sled Distribution, LLC | e7391302-831e-14dc-e053-2a95a90ac236 | 2024-01-15 | Warnings | M017 |
| FIRST SHIELD | LIDOCAINE HCI | Ever Ready First Aid | e022bf8f-3dd8-de22-e053-2995a90a219b | 2024-01-15 | Warnings | M017 |
| Flexigen | MENTHOL 1.25% | Derma Care Research Labs, LLC | e9ae2682-59b4-e796-e053-2995a90af921 | 2024-01-15 | Warnings | M017 |
| Vita-P Oral and Nasal | MENTHOL 1% | Beijing HKKY Medical Tech. Co., Ltd. | 537c3843-1c92-41c6-b724-52701bbddeab | 2024-01-13 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1431703 | menthol 0.15 % Topical Powder | PSN | df1331fb-48df-4f21-8564-0468078fd12d | 4 |
| 1431703 | menthol 0.0015 MG/MG Topical Powder | SCD | df1331fb-48df-4f21-8564-0468078fd12d | 4 |
| 1431703 | menthol 0.15 % Topical Powder | SY | df1331fb-48df-4f21-8564-0468078fd12d | 4 |
| 1431703 | menthol 1.5 MG per GM Topical Powder | SY | df1331fb-48df-4f21-8564-0468078fd12d | 4 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 42669-217-10 | 42669021710 | 283 g in 1 BOTTLE (42669-217-10) | 283 g | 2018-08-22 | 0000-00-00 | No | No | Current |