NDC properties for NDC 9
NDC item 00247054256
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 00247054256 |
NDC item 10223020101
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-1 |
| NDC Item | 10223020101 |
| packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-1) / 56 g in 1 BOTTLE, GLASS |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
NDC item 10223020103
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-3 |
| NDC Item | 10223020103 |
| packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-3) / 20 g in 1 BOTTLE, GLASS |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |
NDC item 10223020104
| NDC 9 | 10223-0201 |
|---|---|
| NDC 10 | 10223-0201-4 |
| NDC Item | 10223020104 |
| packaging | 1 BOTTLE, GLASS in 1 BOX (10223-0201-4) / 5 g in 1 BOTTLE, GLASS |
| Labeler | Cetylite Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time low | 1958-01-01 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_OTHER | N/A |