Ammonia
- Product NDC
- 68599-7100
- 11-digit product format
- 685997100
- Labeler code
- 68599
- Product ID
- 68599-7100_cb090ad6-5323-3f20-e053-2995a90aa2a2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Inhalant
- Dosage form
- AEROSOL
- Route
- RESPIRATORY (INHALATION)
- Labeler
- McKesson
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-01-16
- Marketing end
- 2026-09-01
- Substance
- AMMONIA
- Active strength
- .15 g/g
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ammonia
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMMONIA | .15 g/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5138Q19F1X |
| Rxcui | 1299889 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68599-7100-1 | Ammonia | 0.15 g in 1 BOX | AEROSOL | 0.15 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68599-7100 | AMMONIA (INHALANT) AEROSOL [MCKESSON] | 3 | Current NDC, Legacy NDC, 1 package rows | 20210904_9c4865b7-6d76-7605-e053-2a95a90a1b3f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68599-7100-1 | 68599710001 | .15 g in 1 BOX (68599-7100-1) | 2020-01-16 | 2026-09-01 | No | No | Current |