Liquid Oxygen
- Product NDC
- 70672-002
- Requested package NDC
- 70672-002-01
- 11-digit product format
- 706720002
- Labeler code
- 70672
- Product ID
- 70672-002_5f12fae7-f9ef-f11b-e063-6394a90a86b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Liquid Oxygen
- Dosage form
- GAS
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Dade Medical, Inc. dba Integrated Home Care
- Marketing category
- UNAPPROVED MEDICAL GAS
- Marketing start
- 2026-10-30
- Substance
- OXYGEN
- Active strength
- 99 L/100L
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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
- Liquid Oxygen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXYGEN | 99 L/100L |
Harmonized UNII identifiers#
UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table| Identifier | FDA.report destination |
|---|
| S88TT14065 | Internal UNII lookup |
Harmonized RxCUI identifiers#
RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table| Identifier | FDA.report destination |
|---|
| 312172 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70672-002-01 | 70672000201 | 45 L in 1 DEWAR (70672-002-01) | 45 l | 2026-10-30 | No | No | Current |