warnings
Warnings Use only if cap seal is unbroken. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of the reach of children.
D-136
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- D-136
- Generic name
- SOMATROPIN, LONG-(ARG3)INSULIN-LIKE GROWTH FACTOR-I, ARSENIC TRIOXIDE, SAW PALMETTO, PLATINUM, OYSTER SHELL CALCIUM CARBONATE, CRUDE, BOS TAURUS ADRENAL CORTEX, BOS TAURUS PITUITARY GLAND, POSTERIOR, THYROID, UNSPECIFIED, AND BOS TAURUS HYPOTHALAMUS
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d94be950-ce16-4c55-bbb3-af3f9c4d29d6
- SPL ID
- 2b9efed7-5d89-16bd-e063-6394a90ac14f
- Version
- 3
- Effective date
- 2025-01-13
- Source export date
- 2026-10-27
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:50:45
| Harmonized routes |
|---|
| SUBLINGUAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | D-136 | openfda.brand_name | |
| generic name | SOMATROPIN, LONG-(ARG3)INSULIN-LIKE GROWTH FACTOR-I, ARSENIC TRIOXIDE, SAW PALMETTO, PLATINUM, OYSTER SHELL CALCIUM CARBONATE, CRUDE, BOS TAURUS ADRENAL CORTEX, BOS TAURUS PITUITARY GLAND, POSTERIOR, THYROID, UNSPECIFIED, AND BOS TAURUS HYPOTHALAMUS | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0145-1 | openfda.package_ndc |
| ndc | product | 58264-0145 | openfda.product_ndc |
| ndc11 | package | 58264014501 | derived:openfda.package_ndc |
| spl id | 2b9efed7-5d89-16bd-e063-6394a90ac14f | id | |
| spl set id | d94be950-ce16-4c55-bbb3-af3f9c4d29d6 | set_id | |
| unii | J7WWH9M8QS | openfda.unii | |
| unii | 0B4FDL9I6P | openfda.unii | |
| unii | 7JM57I419K | openfda.unii | |
| unii | NQX9KB6PCL | openfda.unii | |
| unii | 2E32821G6I | openfda.unii | |
| unii | S7V92P67HO | openfda.unii | |
| unii | S6G2NLH4Y7 | openfda.unii | |
| unii | M9L22Y19H9 | openfda.unii | |
| unii | 49DFR088MY | openfda.unii | |
| unii | OWR1Z96774 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.