A and D Original
- Product NDC
- 69213-0096
- Requested package NDC
- 69213-0096-1
- 11-digit product format
- 692130096
- Labeler code
- 69213
- Product ID
- 69213-0096_be3afa7f-b508-46d9-e053-2995a90a2dc1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lanolin and Petrolatum
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Delpharm Montreal Inc.
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2003-06-04
- Marketing end
- 0000-00-00
- Substance
- LANOLIN; PETROLATUM
- Active strength
- 136 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 69213-0096-1 | 69213009601 | 1 TUBE in 1 CARTON (69213-0096-1) > 42.5 g in 1 TUBE | 1 tube | 2003-06-04 | 0000-00-00 | No | No | Current |