Data / Drug companies / Inthismorning Co LTD
Inthismorning Co LTD: 18 products in the FDA NDC directory, labeler code 71217
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Inthismorning Co LTD (labeler code 71217) lists 18 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 18 over the counter drugs. Its main marketing category is other unapproved drugs. The newest product started marketing on January 15, 2023.
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- Labeler code
- 71217
- Products in commercial distribution
- 18
- Packages
- 27
- Finished drugs by generic name
- 9
- Prescription products
- 0
- Over the counter products
- 18
- Flagged as original packager
- 18 of 18 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- January 15, 2023
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Other unapproved drugs | 18 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 18 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Citronellol, geraniol, linalool | 4 | 1 |
| Citronellol | 3 | 1 |
| Limonene | 2 | 1 |
| Oryza sativa (rice) extract | 2 | 2 |
| Niacinamide, adenosine | 2 | 6 |
| Citronellol, geraniol | 2 | 1 |
| Hexyl cinnamal, limonene | 1 | 1 |
| Limonene, linalool | 1 | 1 |
| Citronellol, geraniol, linalool, limonene | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Liquid | 8 | 44.4% |
| Cream | 5 | 27.8% |
| Powder | 3 | 16.7% |
| Gel | 1 | 5.6% |
| Oil | 1 | 5.6% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Standardized Chemical Allergen | 6 |
| Adenosine Receptor Agonist | 3 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Hydrating moisture day and nightcream | 71217-0071 | Cream | Other unapproved drugs | January 15, 2023 |
| Purifying S.O.S spotgel | 71217-0070 | Gel | Other unapproved drugs | January 15, 2023 |
| Claritying rice gently off lip and eye remover | 71217-0066 | Liquid | Other unapproved drugs | January 15, 2023 |
| Claritying rice rebalancing cleansing water | 71217-0065 | Liquid | Other unapproved drugs | January 15, 2023 |
| Intensive treatment bodycream for mommy to be and all skin | 71217-0063 | Cream | Other unapproved drugs | January 15, 2023 |
| Protecting tone up and glow B.B | 71217-0061 | Cream | Other unapproved drugs | January 15, 2023 |
| Protecting base suncream | 71217-0060 | Cream | Other unapproved drugs | January 15, 2023 |
| Protecting natural shine tone up sun cushion | 71217-0059 | Powder | Other unapproved drugs | January 15, 2023 |
| Protecting may morning cushion 21 (refill) | 71217-0058 | Powder | Other unapproved drugs | January 15, 2023 |
| Protecting may morning cushion 21 | 71217-0057 | Powder | Other unapproved drugs | January 15, 2023 |
| Purifying Balance Soothing Peeling Pad | 71217-0055 | Liquid | Other unapproved drugs | January 15, 2023 |
| Purifying relief soothing gel essence | 71217-0054 | Liquid | Other unapproved drugs | January 15, 2023 |
| Purifying centella soothing mask | 71217-0053 | Liquid | Other unapproved drugs | January 15, 2023 |
| Puritying Skin BalanceCream | 71217-0052 | Cream | Other unapproved drugs | January 15, 2023 |
| Hydrating all in one concentrate treatment mask | 71217-0050 | Liquid | Other unapproved drugs | January 15, 2023 |
| Hydrating luxurious roseoil | 71217-0049 | Oil | Other unapproved drugs | January 15, 2023 |
| Hydrating extra concentrate serum | 71217-0048 | Liquid | Other unapproved drugs | January 15, 2023 |
| Hydrating Treatment Toner | 71217-0047 | Liquid | Other unapproved drugs | January 15, 2023 |
CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.